• pesticides
  • Canada has a "Pesticide Risk Reduction Program" where the AAFC (Agriculture and Agri-Food Canada) and the PMRA (Pest Management Regulatory Agency) work to confront the dangers pesticides pose to the environment and human health. (wikipedia.org)
  • products
  • Mylan Inc. ranks among the leading generic and specialty pharmaceutical companies in the world and provides products to customers in more than 150 countries and territories. (bio-medicine.org)
  • That combination is key to assisting clients in bringing their products to market, staying on top of regulatory issues, and responding effectively to matters that may arise over the course of a product's life. (lawbc.com)
  • Dr. Xu's significant experience with FDA regulations and with the Orders and Decrees of the Chinese regulatory system helps him anticipate potential hurdles for clients registering or marketing products in either jurisdiction. (lawbc.com)
  • Bronopol is used in consumer products as an effective preservative agent, as well as a wide variety of industrial applications (almost any industrial water system is a potential environment for bacterial growth, leading to slime and corrosion problems - in many of these systems Bronopol can be a highly effective treatment). (wikipedia.org)
  • Types of pharmaceutical products that may contain tartrazine include vitamins, antacids, cold medications (including cough drops and throat lozenges), lotions and prescription drugs. (wikipedia.org)
  • In addition, products derived from GMO organisms play a role in the production of ethanol fuels and pharmaceuticals. (wikipedia.org)
  • Specific concerns include mixing of genetically modified and non-genetically modified products in the food supply, effects of GMOs on the environment, the rigor of the regulatory process, and consolidation of control of the food supply in companies that make and sell GMOs. (wikipedia.org)
  • The safety assessment of genetically engineered food products by regulatory bodies starts with an evaluation of whether or not the food is substantially equivalent to non-genetically engineered counterparts that are already deemed fit for human consumption. (wikipedia.org)
  • Kallet and Schlink premise the book as being "written in the interest of the consumer, who does not yet realize that he is being used as a guinea pig…" The book's key proposition is that a significant portion of the products sold to the public-particularly pharmaceuticals and food products-are released with little regard for or knowledge of how these products adversely affect the consumer. (wikipedia.org)
  • Preservatives are particularly criticized, and the increase in canned or packaged foods is cited as evidence of an increasing risk of such synergy effects because of the large amount of chemical byproducts these products include. (wikipedia.org)
  • Allergy to Insulin products is rare with a prevalence of about 2%, of which most reactions are not due to the insulin itself but to preservatives added to insulin such as zinc, protamine, and meta-cresol. (wikipedia.org)
  • The Yellow Card Scheme is a United Kingdom initiative run by the Medicines and Healthcare products Regulatory Agency (MHRA) and the Commission on Human Medicines (CHM) to gather information on adverse effects to medicines. (wikipedia.org)
  • product
  • Mylan CEO Heather Bresch said, "We recognize the critical importance of preservative-free Methotrexate Injection in the treatment of patients with cancer, particularly the pediatric population, and share the concerns of patients and physicians about access to this important product. (bio-medicine.org)
  • Pharmaceutical compounding (done in compounding pharmacies) is the creation of a particular pharmaceutical product to fit the unique need of a patient. (wikipedia.org)
  • In terms of drugs, adverse events may be defined as: "Any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and which does not necessarily have to have a causal relationship with this treatment. (wikipedia.org)
  • include
  • Bergeson & Campbell, P.C. (B&C ® ) professionals, who include in-house polymer chemists and other scientists, provide clients the legal and scientific know-how to navigate the regulatory process while keeping an eye on the end-goal of consumer appeal. (lawbc.com)
  • companies
  • In the last decade, substances that may have endocrine effects have been subject to increased regulatory attention, and companies making or using these substances must stay keenly abreast of the sometimes murky and controversial legal and scientific developments regarding endocrine disruptors. (lawbc.com)
  • Pharmacists continued to compound most prescriptions until the early 1950s when the majority of dispensed drugs came directly from the large pharmaceutical companies. (wikipedia.org)
  • It is the largest generic drug manufacturer in the world and one of the 15 largest pharmaceutical companies worldwide. (wikipedia.org)
  • During the 1930s, new immigrants from Europe founded several pharmaceutical companies including Teva ("Nature" in Hebrew), Assia, and Zori. (wikipedia.org)
  • Insulin production from animal pancreases was widespread for decades, but very few patients today rely on insulin from animal sources, largely because few pharmaceutical companies sell it anymore. (wikipedia.org)
  • process
  • The R&D team supports all the development process, including changes in formulation, exploration of Impurities, stability stress-tests, up to the manufacturing of registration batches, ICH regulatory stability studies and over. (epmmagazine.com)
  • The economist Milton Friedman has claimed that the regulatory process is inherently biased against approval of some worthy drugs, because the adverse effects of wrongfully banning a useful drug are undetectable, while the consequences of mistakenly approving a harmful drug are highly publicised and that therefore the FDA will take the action that will result in the least public condemnation of the FDA regardless of the health consequences. (wikipedia.org)
  • Drugs
  • Drugs may be covered by multiple patents or regulatory protections. (drugpatentwatch.com)
  • With the isolation of medications from the raw materials or crude drugs came the birth of the modern pharmaceutical company. (wikipedia.org)
  • The book takes particular aim at the pharmaceutical market in the United States during the period, citing extensive lists of drugs which are often the subject of very strong and widespread campaigns of media promotion as "wonder-drugs," yet which do not have any effect on the conditions they purport to cure, and often carry with them serious side effects that are not revealed to consumers. (wikipedia.org)
  • A $1.8 million 2006 Institute of Medicine report on pharmaceutical regulation in the U.S. found major deficiencies in the FDA system for ensuring the safety of drugs on the American market. (wikipedia.org)
  • drug
  • Attorney Jayne Bultena has almost 20 years of experience in food and drug regulatory matters. (lawbc.com)
  • Pharmaceutical compounding is a branch of pharmacy that continues to play the crucial role of drug development. (wikipedia.org)
  • The Canadian Compendium of Pharmaceuticals and Specialties (CPS), a prescribing reference book for health professionals, mentions tartrazine as a potential allergy for each drug that contains tartrazine. (wikipedia.org)
  • Furthermore, many officials and government departments, namely, the U.S. Food and Drug Administration, have fallen victim to regulatory capture. (wikipedia.org)
  • In 1982, Teva was granted approval by the U.S. Food and Drug Administration (FDA) for its Kfar Saba manufacturing plant, an essential milestone for marketing pharmaceuticals in the US. (wikipedia.org)
  • increase
  • Mylan has already ramped up its production in order to try to meet the increased demand and is aggressively working on both the manufacturing and regulatory fronts to expedite the FDA regulatory approvals necessary to further increase capacity. (bio-medicine.org)
  • Overall, the authors called for an increase in the regulatory powers, funding, and independence of the FDA. (wikipedia.org)
  • safety
  • Layered atop these decisions are a host of regulatory issues, including packaging safety to labeling accuracy. (lawbc.com)
  • Mass
  • WALTHAM, Mass., Nov. 3, 2015 (GLOBE NEWSWIRE) -- AMAG Pharmaceuticals, Inc. (NASDAQ:AMAG) today reported unaudited consolidated financial results for the third quarter and year-to-date periods ended September 30, 2015. (cnbc.com)
  • paid
  • In June 2013 Teva acquired US firm MicroDose for $40 million with as much as $125 million being paid in regulatory and developmental milestones In 2010, Teva announced that it would build its main distribution center for the Americas in Philadelphia, PA, and was considering opening its US headquarters in the area. (wikipedia.org)
  • professionals
  • It is these 'grass roots' pharmaceutical professionals who can often provide a reasoned and dare I say it, an impartial view when a European Directive has been circulated for consultation. (issuu.com)
  • status
  • The legal and regulatory status of GM foods varies by country, with some nations banning or restricting them, and others permitting them with widely differing degrees of regulation. (wikipedia.org)