French agency for veterinary medicinal products. Medical search. Frequent questions

The Committee adopted by consensus a positive opinion for an initial marketing authorisation application for Stronghold Plus ( selamectin/sarolaner ), from Zoetis Belgium SA, a new antiparasitic product for cats . (europa.eu)
The event will also highlighted the tools already available in the Regulation to facilitate the marketing authorisation of new veterinary medicinal products or introduce variations in the authorisation of those already registered for other indications and/or species. (resistenciaantibioticos.es)
The goal is to be able to provide global solutions to pharmaceutical companies, either on an ad hoc basis, or by offering a turnkey service of the product, including galenic and stability developments, marketing authorisation applications, purchases, production and regulatory affairs. (le70e-normandie.fr)
The development of a harmonised, EU level guidance on data integrity is the tool identified by the GMDP IWG to reinforce responsibility of marketing authorisation holders (MAHs) for product quality. (eipg.eu)
MEB is responsible for the authorisation of safe and effective medicinal products and for their subsequent monitoring on the Dutch market, and does this by providing scientific advice, assessing marke. (bvs.br)
Previously, a systematic approach had been used, i.e. each yearly programme included products that had been granted a community market authorisation 3 years previously. (edqm.eu)
However, when the medicinal product is a generic (1) or biosimilar (2) product, a company can avoid having to carry out full trials by relying on at least some of the data submitted by the original applicant for marketing authorisation in connection with the original (reference) medicinal product. (dehns.com)
In an attempt to harmonise the position in Europe and to speed up the entry of generic products onto the market after patent expiry, the so called "Bolar exemption" was introduced by the European Union (EU) to exempt from patent infringement the tests and trials necessary to use the abridged procedure for obtaining marketing authorisation. (dehns.com)
A particularly contentious issue is whether a third party is free to supply the medicinal product to the party carrying out the trials necessary to obtain marketing authorisation. (dehns.com)
It is recognised that allowing the producer of a generic or biosimilar medicinal product to use an abridged marketing authorisation gives the producer of the generic or biosimilar an advantage. (dehns.com)
Detailed further information regarding these forms of exclusivity, as well as regarding the requirements for obtaining marketing authorisation for generics and biosimilars may be found on the website of the European Medicines Agency. (dehns.com)
It explains how the Committee for Medicinal Products for Human Use ( CHMP ) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Byetta. (europa.eu)
For centrally authorised medicinal products the MAH will therefore normally need to transfer its marketing authorisation to a holder established in the EU (EEA). (hcltech.com)
The competent authorities of the Union (EEA) shall ensure that the import of medicinal products into their territory is subject to an authorisation in accordance with the EU directives on importation (See the Q&A article for full detail). (hcltech.com)

WHO prequalification encourages international collaboration and harmonization of standards for the manufacture, quality control, regulation and monitoring of medicines, vaccines and other health products. (who.int)
The European Medicines Agency (EMA) published a draft reflecting paper on July 19, 2023 detailing the agency's current outlook on the use of artificial intelligence (AI) "to support the safe and effective development, regulation and use of human and veterinary medicines. (pharmtech.com)
The EU institutions agreed on a Regulation on advanced therapies (Regulation (EC) 1394/2007 ), designed to ensure the free movement of advanced therapy products within Europe, to facilitate access to the EU market and to foster the competitiveness of European companies in the field, while guaranteeing the highest level of health protection for patients. (genetherapynet.com)
whose organisations are responsible for the regulation of medicinal products for human and veterinary use in the European Economic Area. (hma.eu)
Member agencies support the network by providing high-quality professional and scientific resources to all areas of medicines regulation including centralised, MRP , DCP and national procedures. (hma.eu)
ANSES is committed to ensuring that the processing of personal data on the www.anses.fr site complies with the General Data Protection Regulation (GDPR) and the French Data Protection Act. (anses.fr)
In the United States , 47 states out of 50 have allowed the use of CBD products with varying degrees of regulation. (cbdclinicals.com)
The implementation of the new Veterinary Regulation should be addressed paying attention both to GDP for veterinary medicines and active substances. (eipg.eu)
To this regard, suggested actions include the support to the international API programme , comprehensive of the provisions of the new Veterinary Regulation related to API inspections and controls. (eipg.eu)
Medsafe is the agency responsible for the regulation of medicines and medical devices in New Zealand, and the safe use of medicines. (bvs.br)
MPA is the Swedish national authority responsible for regulation and surveillance of the development, manufacturing and sale of drugs and other medicinal products. (bvs.br)
The fundamental role of the IMB is to protect and enhance public and animal health through the regulation of human and veterinary medical products. (bvs.br)

A Working Group to promote the availability of veterinary medicinal products containing antimicrobials and alternatives to their use is currently working, as part of National Action Plan on Antimicrobial Resistance (PRAN) in Spain, with the aim of mitigating the existing therapeutic gaps and lack of alternatives present in veterinary medicine, particularly in those species considered as minor. (resistenciaantibioticos.es)
The products in scope include sterile medicines for human use of chemical origin and certain therapeutic biotechnology-derived products, such as monoclonal antibodies and recombinant proteins. (who.int)
Treatment, control and prevention are collectively defined as 'therapeutic use' by international institutions such as the World Health Organization (WHO), United Nations' Food and Agriculture Organization (FAO) and World Organisation for Animal Health (WOAH) as well as by government regulatory agencies such as the United States Food and Drug Administration (US FDA) and European Medicines Agency's Committee for Veterinary Medicinal Products (EU/EMA/CVMP). (elanco.com)
These products were developed expressly for therapeutic use in animals and are not useful in human medicine. (elanco.com)
This constitutes a clear deviation from and rejection of an interpretation of an earlier decision (ECJ, judgment of 07/19/2012 "Neurim Pharmaceuticals", C-130/11), which stated that an earlier veterinary marketing authorization of an active substance would allow the granting of an SPC for another therapeutic application of the same active ingredient. (maucherjenkins.com)

The risk of development of AMR is caused by two major pathways: the lack of alternatives to prevent the use of antimicrobials, such as vaccines, and the small number of veterinary medicinal products with antimicrobials available, which avoids the use of the best alternative and prevents the rotation of active substances, increasing the risk of selection of resistant organisms. (resistenciaantibioticos.es)
Replace antibiotics with alternatives - Elanco has intentionally expanded our vaccine and nutritional health capabilities since 2015 to provide alternative solutions - including nutritional health products like enzymes, probiotics and prebiotics, parasiticides and vaccines. (elanco.com)
IDT Biologika, a globally integrated manufacturer of vaccines and biopharmaceuticals, announced today that the National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health (NIH), an agency of the United States Department of Health and Human Services, has awarded the company a new Task Order within the 10-year Indefinite Delivery, Indefinite Quantity (IDIQ) contract no. (idt-biologika.com)
Recently the company announced that it is to concentrate on human vaccines and biologics, having transferred the animal health business to the French veterinary health group Ceva Santé Animale. (idt-biologika.com)
IDT Biologika offers global expertise from an almost century of experience in vaccine development and manufacture and now specializes in the contract development and manufacturing of vaccines, gene therapy medicinal products, sterile liquids and lyophilized biologics. (idt-biologika.com)
Procedure for assessing the acceptability, in principle, of vaccines for purchase by United Nations agencies. (who.int)

The Committee adopted by consensus an opinion concluding that overall the benefit-risk balance for the products concerned by this referral is negative, as the benefits of zinc oxide for the prevention of diarrhoea in pigs do not outweigh the risks for the environment. (europa.eu)
The laboratory's mission is to further knowledge of the benefits and risks of veterinary medicinal product and disinfectant use by the food processing industry. (anses.fr)
The Agency also assesses the effectiveness and risks of veterinary medicinal products, plant protection products, fertilisers, growing media and their adjuvants, as well as biocides, with a view to delivering marketing authorisations. (hal.science)
BfArM is an independent higher federal authority within the portfolio of the Federal Ministry of Health, and has the aim of preventing health risks by continuous improvement in the safety of medicinal. (bvs.br)

The main types of drugs classes in veterinary anti-infectives are antimicrobial agents, antiviral agents, antifungal agents, and others. (thebusinessresearchcompany.com)
The laboratory is the National Reference Laboratory for veterinary medicine residues and antimicrobial resistance. (anses.fr)
His Excellency the Governor General in Council, on the recommendation of the Minister of Health, pursuant to subsection 30(1) (see footnote a) of the Food and Drugs Act (see footnote b) , makes the annexed Regulations Amending the Food and Drug Regulations (Veterinary Drugs - Antimicrobial Resistance) . (gc.ca)

Other markets driving the market include dangers of human pharmaceutical compounds as well as veterinary pharmaceutical compounds falling in drinking water resources, standards set by environmental regulatory authorities, and government initiatives for creating awareness. (medgadget.com)
PIC/S is a non-binding, informal co-operative arrangement between regulatory authorities in the field of good manufacturing practice (GMP) for medicinal products for human or veterinary use. (who.int)
It was creative collaboratively by the BDSG, EMA's Committee for Medicinal Products for Human Use and its Committee for Veterinary Medicinal Products. (pharmtech.com)
Anses (The French Agency for Food, Environmental and Occupational Health & Safety) undertakes monitoring, expert assessment, research and reference activities in a broad range of topics that encompass human health, animal health and well-being, and plant health. (hal.science)
Human infections have been reported mainly in persons handling infected animals and their products ( 5 - 8 ). (cdc.gov)
Volume 10 - Clinical trials guidelines contains guidance documents concerning medicinal products for human use in clinical trials (investigational medicinal products). (genetherapynet.com)
The EU Clinical Trials Directive establishes specific provisions regarding the conduct of clinical trials, including multi-centre trials, on human subjects involving medicinal products in particular relating to the implementation of good clinical practice. (genetherapynet.com)
As regards the term 'medicinal products', this refers to medicinal products for human use as defined in Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use. (genetherapynet.com)
The CDMO is intended for all areas of the pharmaceutical industry, medicines and medical devices for use in human or veterinary medicine and dermocosmetics. (le70e-normandie.fr)
The Heads of Medicines Agencies would like to reiterate the paramount importance for all involved to prepare for withdrawal in the interest European human and animal health. (hma.eu)
It is therefore necessary to ensure that the anti-lice products used in human medicine and especially in children, really are medicines authorised for human use. (famhp.be)
The Committee for Medicinal Products for Human Use of the European Medicines Agency has begun the analyse of the results of the independent epidemiological study funded by the European Commission to better assess the risk of gastro-intestinal and cardiovascular toxicity of non-selective NSAIDs. (famhp.be)
The Committee for Medicinal Products for Human Use of the European Medicines Agency points out the opinion issued in July 2011 for pioglitazone. (famhp.be)
Strategical goals include the enhancement of traceability, oversight and security for both the human and veterinary medicine supply chain. (eipg.eu)
The CJEU does not state that Neurim is limited to its facts (i.e. veterinary-to-human), but the reasoning indicates that the direction of travel is a very narrow approach. (blogspot.com)
This raises question marks for strategies that have been deployed seeking SPCs in reliance on Neurim, in particular those that do not have the veterinary-to-human facts. (blogspot.com)
Since 1995, the Commission of the European Union has being granting community marketing authorisations for new medicines for both human and veterinary use. (edqm.eu)
Since its initiation, the programme - originally covering 'regular' medicinal products for human and veterinary use and generics - has been continuously improved thanks to the close collaboration between its partners. (edqm.eu)
The 2022 CAP Regular programme included 33 medicinal products for human use (19 biologicals, including two insulin-based products, and 14 chemical products) and seven medicinal products for veterinary use (four immunobiological products and three chemical products). (edqm.eu)
The Bolar exemption is governed by European Directive 2001/83/EC on the Community Code relating to medicinal products for human use, as amended by European Directive 2004/27/EC, particularly Article 10 thereof. (dehns.com)
In response to emerging developments, the recent resolutions 781 of 2022 and modification of Resolution 767/2023 address cannabis-based products for human medicinal use, establishing a distinct category while building upon existing TCM regulations. (bvsalud.org)

The global veterinary anti-infectives market size will grow from $4.64 billion in 2022 to $5.08 billion in 2023 at a compound annual growth rate (CAGR) of 9.6% . (thebusinessresearchcompany.com)
In June 2022, Ceva Santé Animale, a France-based multinational animal health company, acquired Artemis Technologies, Inc for an undisclosed amount. (thebusinessresearchcompany.com)
For instance, in October 2022, according to Eurostat, a Luxembourg-based agency of the European Commission, in 2021, Europe's pig meat production was 23.4 million metric tons. (thebusinessresearchcompany.com)
Furthermore, according to the Food and Agriculture Organization, an Italy-based United Nations specialized agency, worldwide dairy output reached 930 million tons in 2022, a 0.6% rise from 2021. (thebusinessresearchcompany.com)
The 2022 CAP Generics surveillance programme covered products containing imatinib, memantine and pregabalin. (edqm.eu)
The results of the 2022 programmes showed that the vast majority of products tested were of the expected quality and complied with the authorised specifications. (edqm.eu)

Following the Committee's review of a request for classification under the MUMS/limited market policy, the CVMP classified an indication for an anti-parasitic veterinary product for dogs as indicated for MUMS/limited market and eligible for reduced data requirements. (europa.eu)

In response to the increasing number of biosimilars, a five-year (2019-2023) Biosimilar programme , comprising three projects on CAP products containing filgrastim, etanercept and rituximab, is currently ongoing. (edqm.eu)
Thus, whilst some countries, notably the UK, have adopted an exemption that is limited to generic or biosimilar medicinal products, others, including Germany and France, have adopted an exemption that is not so limited, extending also to innovative medicinal products. (dehns.com)
In addition, a further period of "market exclusivity" runs from the end of the data exclusivity period and prevents manufacturers of generic/biosimilar medicinal products from placing their products onto the market. (dehns.com)

This includes medicinal products where the pharmacological, immunological, or metabolic action of the product is still uncertain and being explored. (genetherapynet.com)

Afssaps is the french competent authority for all safety decisions taken concerning health products from their manufacturing to their marketing, and carries out three core missions: scientific and med. (bvs.br)
On June 3, 2015, Santen applied for an SPC for a product called "Cyclosporin for use in the treatment of corneal inflammation" at the competent office in France, the INPI. (maucherjenkins.com)

The matter was referred to the Committee by the Netherlands and France under Article 35 of Directive 2001/82/EC due to concerns related to potential risk to the environment and increase of prevalence of antibiotic resistant bacteria from the use of products containing zinc oxide. (europa.eu)
The Committee therefore recommended the refusal of the granting of the marketing authorisations and the withdrawal of the existing marketing authorisations for veterinary medicinal products containing zinc oxide. (europa.eu)
The Committee adopted one scientific advice report further to a request for initial advice on MRL issues for a new veterinary medicinal product for broilers. (europa.eu)
The Committee also reviewed the PSURs for Easotic , Loxicom and Rheumocam , and recommended amendments to their product literature. (europa.eu)
Staphylococcus aureus isolates were confirmed by polymerase chain reaction (PCR) amplification of the nuc gene, and the antibiogram was performed according to the guidelines of the Antibiogram Committee of the French Society of Microbiology (CA-SFM 2021). (bvsalud.org)

The HMA co-operates with the European Medicines Agency (EMA) and the European Commission in the operation of the European medicines regulatory network and it is a unique model for cooperation and worksharing on statutory as well as voluntary regulatory activities. (hma.eu)
For centrally authorised products please find guidance by the European Medicines Agency and European Commission here . (hma.eu)
actions to prevent medicine shortages due to Brexit please find the information prepared by the European Medicines Agency here . (hma.eu)
Evaluation of statistics and methods of applications for approval of drugs in collaboration with national regulatory agencies and the European Medicines Agency (EMA). (wilmarigl.de)
The European Medicines Agency has released the input notes made by the GMDP Inspectors Working Group (IWG) as for the drafting of the 3-year workplan for the Quality domain . (eipg.eu)
In June 1999, a contract governing an annual CAP Sampling & Testing Programme was signed by the European Medicines Agency ( EMA ) and the EDQM . (edqm.eu)
Santen had received marketing authorization from the European Medicines Agency (EMA) on March 19, 2015 for the treatment of severe corneal inflammation in adults with dry eyes after certain failed previous treatments. (maucherjenkins.com)

These are known as centrally authorised products ( CAP ). (edqm.eu)
The concerted Centrally Authorised Products (CAP) Sampling & Testing programme has entered its 24th consecutive year . (edqm.eu)

During the marketing-authorization stage, AI has tools to draft, compile, translate, or review data that are used in the product information of a medicine. (pharmtech.com)
The Fougères Laboratory operates in the areas of food safety, veterinary medicine and food hygiene. (anses.fr)
This solid performance was led by the strong growth of companion animal products Revolution, Rimadyl, and Clavamox/Synulox and of the livestock medicine RespiSure/Stellamune. (brakkeconsulting.com)
NCCAM is the U.S. Federal Government's lead agency for scientific research on complementary and alternative medicine (CAM), and sponsors and conducts research using scientific methods and advanced tec. (bvs.br)

Advanced therapy medicinal products (ATMPs) are new medical products based on genes (gene therapy), cells (cell therapy) and tissues (tissue engineering). (genetherapynet.com)

PIC/S and the International Coalition of Medicines Regulatory Agencies (ICRMA) should also collaborate with the GMDP IWG to reach an agreement on shared definitions, best practices and harmonised approaches for distant assessment and hybrid inspections . (eipg.eu)

In order to promote and support these principles WHO prequalification participates as an observer in relevant international fora and has signed collaboration agreements with several organizations, agencies and national regulatory authorities. (who.int)
The EU also provides an overview of national regulatory requirements (EU countries and Norway) for medicinal products containing GMOs. (genetherapynet.com)

Long-acting orally administered products overcome these shortcomings with the added advantage of potential to kill fleas more rapidly than topically applied flea control products, possibly because of the time needed for a topically applied product to homogeneously distribute from the site of application to the whole-body surface [ 2 , 3 ]. (biomedcentral.com)

Moreover, all of the notices and reports produced by the Agency since it was created are now available on-line in full-text form on the Anses website . (hal.science)
The www.anses.fr website is managed by the French Agency for Food, Environmental and Occupational Health & Safety (ANSES). (anses.fr)
The Federal Agency for Medicines and Health Products (FAMHP) was informed by the French National Agency of Sanitary Safety (ANSES) about the improper use of certain medicines (particularly those containing fipronil) for veterinary used to treat pediculosis (lice infestation) in children. (famhp.be)

Lotilaner was well tolerated, with no product-related adverse events reported. (biomedcentral.com)
But he also has to deal with the economic damage caused by the adverse weather conditions (mainly rains) resulting in the quality degradation of the products due to disease attacks. (edu.gr)

To meet with pharmaceutical industry requirements, contract manufacturers must comply with recommendations from the pharmacovigilance agencies of the host country where the manufacturing site is located. (le70e-normandie.fr)

It is also common to outsource analytical development, conduct of clinical trials and studies on the stability of the medicinal product. (le70e-normandie.fr)
In order to market a medicinal product, a manufacturer must first obtain regulatory approval by conducting clinical tests and trials to prove that the product is safe and effective. (dehns.com)
It is widely accepted that actual trials testing the safety or efficacy of the medicinal products would fall within the scope of this exemption, but there has been uncertainty regarding other acts, such as the manufacture, supply or import of the medicinal product. (dehns.com)
I run trials of bee health products for companies wishing to bring new products to market. (scientificbeekeeping.com)

This product is designed for veterinary use and tulathromycin, the active ingredient in Increxxa, helps decrease the negative effects of bovine respiratory disease. (thebusinessresearchcompany.com)
Additional active pharmaceutical ingredient (API) or medicinal product intermediate testing was performed for four products. (edqm.eu)
This was rejected because on December 23, 1983 a marketing authorization for a product called "Sandimmun" containing cyclosporine as an active ingredient had already been granted. (maucherjenkins.com)
The event will also look at January's Forsgren (C-631/13) judgment (discussed here ), which has profound things to say on the way active ingredients can be protected by SPCs, particularly for complex biologic products. (blogspot.com)

Medicinal products for paediatric use, orphan, herbal medicinal products and advanced therapies are governed by specific rules. (genetherapynet.com)
The regulatory requirements for the safety assessment of herbal medicines include reference to safety data in documented scientific research on similar products and toxicity studies. (bvsalud.org)

For instance, in July 2021, Light Science Technologies, a UK-based developer of controlled-environment agriculture products, launched NurturGrow LED grow lights. (thebusinessresearchcompany.com)

The term veterinary anti-infective refers to a broad category where animals are cared for by providing both illness prevention and cure approaches. (thebusinessresearchcompany.com)
Livestock productivity refers to how efficiently and effectively livestock are raised to produce various outputs such as meat, milk, eggs, wool, and other animal products. (thebusinessresearchcompany.com)

Veterinary specific GMP guideline annexes 4 and 5 should be harmonised in collaboration with PIC/S. The collaboration should also include ongoing initiatives on inspection reliance , in order to better identify barriers preventing member states from accepting inspection results from other trusted authorities. (eipg.eu)

The market size of veterinary anti-infectives is expected to grow to $7 billion in 2027 at a CAGR of 8.3% . (thebusinessresearchcompany.com)
An increase in pet ownership is expected to propel the growth of the veterinary anti-infectives market going forward. (thebusinessresearchcompany.com)
Therefore, an increase in pet ownership is driving the demand for veterinary anti-infectives market. (thebusinessresearchcompany.com)
Technological advancements are a key trend gaining popularity in the veterinary anti-infectives market. (thebusinessresearchcompany.com)
Major companies operating in the market are using advanced technologies to sustain their position in the veterinary anti-infectives market. (thebusinessresearchcompany.com)
Depending on the company's needs, contract manufacturers can step in at the early stage of researching a molecule or at the time of packaging before products become available on the market. (le70e-normandie.fr)
Product innovations are a key trend gaining popularity in the livestock grow lights market. (thebusinessresearchcompany.com)
Major companies operating in the livestock grow lights market are introducing innovative products related to sustainable LED grow lights to sustain their position in the market. (thebusinessresearchcompany.com)
In addition, new products with altered formulations are predicted to meet market demands. (cbinsights.com)
Additionally, it is anticipated that rising anti-VEGF agent demand and usage, as well as the existence of significant market players with broad product portfolios, would all contribute to the segment's expansion. (cbinsights.com)
National inspection services gather sample products from the market and members of the EU/EEA OMCL Network test them. (edqm.eu)
The decision in T-140/12 is fascinating, as it appears to mean that the (co-)exclusivity awarded to one product can effectively extend the period of (co-)exclusivity on the market for another, "similar" product. (blogspot.com)
6. 'Market price' is the price, written on the excise label, at which tobacco products are sold at retail price to an end consumer. (who.int)

Since 2009, each annual programme has included products selected using a risk-based approach. (edqm.eu)
The list of products to be included in the annual programme is prepared by the EMA Secretariat in collaboration with the EMA Scientific Committees. (edqm.eu)
A list of products to be included in the annual Regular programme is jointly prepared by the EMA Secretariat and the EMA Scientific Committees, with input from the OMCL Network and the EDQM, applying a risk-based approach. (edqm.eu)
Finally, N-nitrosamine testing has been added to the programme for some selected products. (edqm.eu)

The document identifies a number of strategic goals aimed at improving the overall integrity and resilience of the pharmaceutical supply chain and the product quality, and to optimise the im-pact of new technologies. (eipg.eu)

The product is not eligible for financial incentives as it is intended for use in a non-food producing species. (europa.eu)
The various species types involved are livestock animals and companion animals that are administered through oral, parenteral, and topical modes of administration and are distributed through veterinary hospitals, veterinary clinics, pharmacies, and other distribution channels. (thebusinessresearchcompany.com)

The selling of ingestible CBD products often requires a food-specific business license (14) . (cbdclinicals.com)
What does the Agency do to ensure that food is safe? (anses.fr)
The Agency takes action, "from farm to fork", to ensure food safety. (anses.fr)
Read our 10 recommendations (PDF) to avoid food poisoning (in French). (anses.fr)

Moreover, the laboratory develops new tools for predicting the toxicity of these products. (anses.fr)

Inspections are most notably carried out by the ANSM in France and the FDA in the United States. (le70e-normandie.fr)

The livestock productivity can be increased using livestock grow lights, which facilitate the growth and production of animal products by emitting light that emulates natural light and creates a physiological effect on livestock. (thebusinessresearchcompany.com)

The term 'antibiosis', meaning "against life", was introduced by the French bacteriologist Jean Paul Vuillemin as a descriptive name of the phenomenon exhibited by these early antibacterial drugs. (wikipedia.org)
The product type segment is OTC Drugs and prescription drugs. (cbinsights.com)
The lubricating and moisturising components in several medicinal drugs temporarily boost the production of tears. (cbinsights.com)

The mission of PIC/S is to lead the international development, implementation and maintenance of harmonized GMP standards and quality systems of inspectorates for medicinal products. (who.int)

For products authorised in decentralised or mutual recognition procedures please find guidance by CMDh here and CMDv here . (hma.eu)

In conclusion, delegating the manufacture of pharmaceutical products and accessories to a contract manufacturer forms part of a strategic approach. (le70e-normandie.fr)

We may know more on this issue soon given the pending referral from the French courts in Santen ( C-673/18 ). (blogspot.com)

In accordance with the provisions of Article 56 of French Act No 78-17 of 6 January 1978 on information technology, files and freedoms, you can contact the Data Protection Officer (DPO) to object to the processing of your data. (anses.fr)

Their treatment contributes significantly to the increase in production costs and the burden on the environment with chemical compounds (plant protection products). (edu.gr)

It allows the partial or complete transfer of development and production of a product or a medical device. (le70e-normandie.fr)
The availability and legalization of CBD and other cannabis-derived products are scarce in Asia, with only a few countries, such as Thailand (2) , legalizing the use of medical cannabis and the use of CBD in cosmetics. (cbdclinicals.com)
The Federal Agency for Medicines and Health Products (FAMHP) confirms that the premature baby bottles for single use sterilized with ethylene oxide (ETO called), used in hospitals are notified as medical devices. (famhp.be)
The review should be aimed to the identification of sites manufacturing a significant number of products or producing medical pro-ducts for a significant number of markets within the European economical area (EEA). (eipg.eu)

It has separately been developed for oral administration in cats (Credelio™ chewable tablets for cats) to meet the need for an easy to use, safe and rapidly effective parasiticide and as an alternative to topical products. (biomedcentral.com)

Technical requirements adapted to the particular characteristics of these products. (genetherapynet.com)
Leading institutions such as EKETA and the American School of Agriculture cooperate with a table grape grower of the Crimson seedless variety of Northern Greece in order to give this particular exportable variety increased credibility in terms of quality specifications and, combined with their excellent organoleptic characteristics, to reduce it to emblematic product of Greek fresh fruit exports. (edu.gr)

Some are based on sodium chlorite that is activated into chlorine dioxide, though differing formulations are used in each product. (wikipedia.org)

A number of new products were launched in key markets, and the farm animal segment benefited from the recovery of the UK foot and mouth epidemic. (brakkeconsulting.com)
The new product is innovative and sustainable, with 85% of its reusable components, which would help animal farmers and indoor growers upgrade the features quickly and save on lighting costs. (thebusinessresearchcompany.com)

Many other products on the EPA list contain sodium hypochlorite, which is similar in name but should not be confused with sodium chlorite because they have very different modes of chemical action. (wikipedia.org)

This overview has been developed in 2018 as a result of joint efforts to harmonize between the GMO legislation and the legislation on medicinal products. (genetherapynet.com)

Topical flea control products have to be applied carefully directly to the pet's skin and can potentially lead to pesticide exposure of all household members. (biomedcentral.com)

Many laboratories today use outsourcing to optimise their pharmaceutical product development. (le70e-normandie.fr)

Albania Austria Bangladesh Belgium Bosnia-Herzegovina Brazil British Indian Ocean Territory Bulgaria Cambodia Canada Chile China Colombia Costa Rica Croatia Czech Republic Denmark Egypt El Salvador France Germany Greece Guatemala Honduras Hong Kong India Indonesia Italy Kosovo Lao people's democratic rep. (sa-intl.org)

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