EudraLex – Volume 4 Good manufacturing practice (GMP) Guidelines #app #pharma

Posted On Sep 9 2017 by

#gmp pharma # European Commission Public health EudraLex – Volume 4 Good manufacturing practice (GMP) Guidelines. Volume 4 of “The rules governing medicinal products in the European Union” contains guidance for the interpretation of the principles and guidelines of good manufacturing practices for medicinal products for human and veterinary use laid down in Commission Directives 91/356/EEC, as amended by Directive 2003/94/EC, and 91/412/EEC respectively. Introduction Introduction (33 KB) (7/02/2011) Commission Directive 2003/94/EC. of 8 October 2003, laying down the principles and guidelines of good manufacturing practice in respect of medicinal products for human use and investigational medicinal products for human …


What the Latest FTC Guidelines Mean to Pharma Marketers #canadian #pharma

Posted On Aug 29 2017 by

#pharma guidelines # What the Latest FTC Guidelines Mean to Pharma Marketers As pharma marketers, we tend to listen closely when the U.S. Food and Drug Administration (FDA) issues guidance, such as their draft guidance on correcting misinformation online. and user-generated content. In June this year, however, it was guidelines from the Federal Trade Commission (FTC) that got our attention. The updates published via the agency s frequently asked questions and social media marketing guidelines focus primarily on testimonials and endorsements. With the rise in popularity of product reviews, the FTC is interested in ensuring consumers can clearly tell the …


EudraLex – Volume 4 Good manufacturing practice (GMP) Guidelines #pharmaceuticals #industry

Posted On Aug 29 2017 by

#gmp pharma # European Commission Public health EudraLex – Volume 4 Good manufacturing practice (GMP) Guidelines. Volume 4 of “The rules governing medicinal products in the European Union” contains guidance for the interpretation of the principles and guidelines of good manufacturing practices for medicinal products for human and veterinary use laid down in Commission Directives 91/356/EEC, as amended by Directive 2003/94/EC, and 91/412/EEC respectively. Introduction Introduction (33 KB) (7/02/2011) Commission Directive 2003/94/EC. of 8 October 2003, laying down the principles and guidelines of good manufacturing practice in respect of medicinal products for human use and investigational medicinal products for human …


Editorial Guidelines – Contract Pharma #major #pharmaceutical #companies

Posted On Aug 18 2017 by

#pharma guidelines # Editorial Guidelines Author Guidelines for Submitting Content to Contract Pharma Contract Pharma welcomes opinion pieces, blog posts and articles on any relevant aspects of pharmaceutical and biopharmaceutical contract services and outsourcing. These include, but are not limited to, Quality Control and Assurance, manufacturing of various dosage forms, R D, clinical trial supplies and clinical studies outsourcing, packaging, drug discovery, regulatory affairs, analytical testing, methods/process validation, formulation development, technology transfer, and others. Here are some suggestions. 2. Please keep the article conversational in tone, without academic journal style or use of passive voice Articles can and should get …


Editorial Guidelines – Contract Pharma #cardiome #pharma

Posted On Aug 10 2017 by

#pharma guidelines # Editorial Guidelines Author Guidelines for Submitting Content to Contract Pharma Contract Pharma welcomes opinion pieces, blog posts and articles on any relevant aspects of pharmaceutical and biopharmaceutical contract services and outsourcing. These include, but are not limited to, Quality Control and Assurance, manufacturing of various dosage forms, R D, clinical trial supplies and clinical studies outsourcing, packaging, drug discovery, regulatory affairs, analytical testing, methods/process validation, formulation development, technology transfer, and others. Here are some suggestions. 2. Please keep the article conversational in tone, without academic journal style or use of passive voice Articles can and should get …


Editorial Guidelines – Contract Pharma #pharmaceuticals #companies

Posted On Aug 3 2017 by

#pharma guidelines # Editorial Guidelines Author Guidelines for Submitting Content to Contract Pharma Contract Pharma welcomes opinion pieces, blog posts and articles on any relevant aspects of pharmaceutical and biopharmaceutical contract services and outsourcing. These include, but are not limited to, Quality Control and Assurance, manufacturing of various dosage forms, R D, clinical trial supplies and clinical studies outsourcing, packaging, drug discovery, regulatory affairs, analytical testing, methods/process validation, formulation development, technology transfer, and others. Here are some suggestions. 2. Please keep the article conversational in tone, without academic journal style or use of passive voice Articles can and should get …


Confused Over New Pharma Guidelines? GCG Event Partners #arch #pharma

Posted On Jul 25 2017 by

#pharma guidelines # Confused Over New Pharma Guidelines? Yes, it’s tax time again. And if you lose sleep just thinking about a potential audit of your own personal income because you might possibly have stretched the truth just a teensy bit about some business deductions you made last year well, consider yourself lucky you re not a meeting planner for one of the big pharmaceutical companies. It s possible they re all sleep deprived now that the Physician Payment Sunshine Act (PPSA) has taken effect. Thanks to PPSA, a key part of the federal Affordable Care Act of 2010, meeting …


Editorial Guidelines – Contract Pharma #pharma #manufacturers

Posted On Jul 25 2017 by

#pharma guidelines # Editorial Guidelines Author Guidelines for Submitting Content to Contract Pharma Contract Pharma welcomes opinion pieces, blog posts and articles on any relevant aspects of pharmaceutical and biopharmaceutical contract services and outsourcing. These include, but are not limited to, Quality Control and Assurance, manufacturing of various dosage forms, R D, clinical trial supplies and clinical studies outsourcing, packaging, drug discovery, regulatory affairs, analytical testing, methods/process validation, formulation development, technology transfer, and others. Here are some suggestions. 2. Please keep the article conversational in tone, without academic journal style or use of passive voice Articles can and should get …


What the Latest FTC Guidelines Mean to Pharma Marketers #pharma #manufacturer

Posted On Jul 11 2017 by

#pharma guidelines # What the Latest FTC Guidelines Mean to Pharma Marketers As pharma marketers, we tend to listen closely when the U.S. Food and Drug Administration (FDA) issues guidance, such as their draft guidance on correcting misinformation online. and user-generated content. In June this year, however, it was guidelines from the Federal Trade Commission (FTC) that got our attention. The updates published via the agency s frequently asked questions and social media marketing guidelines focus primarily on testimonials and endorsements. With the rise in popularity of product reviews, the FTC is interested in ensuring consumers can clearly tell the …


Confused Over New Pharma Guidelines? GCG Event Partners #best #pharma #companies

Posted On Jul 11 2017 by

#pharma guidelines # Confused Over New Pharma Guidelines? Yes, it’s tax time again. And if you lose sleep just thinking about a potential audit of your own personal income because you might possibly have stretched the truth just a teensy bit about some business deductions you made last year well, consider yourself lucky you re not a meeting planner for one of the big pharmaceutical companies. It s possible they re all sleep deprived now that the Physician Payment Sunshine Act (PPSA) has taken effect. Thanks to PPSA, a key part of the federal Affordable Care Act of 2010, meeting …