image image image
Industrial Pharmacy If you are a pharmaceutical scientist or executive working in or liaising with Industry, your job will be made easier, more productive and more enjoyable by reading Industrial Pharmacy.

The journal covers a variety of topics of interest to those working in the worldwide pharma industry (for Contents of the current issue, please click on the pdf below). Industrial Pharmacy is published four times a year.

Learn more
GMP Review A quarterly publication researched and edited by an expert team experienced in all aspects of pharmaceutical manufacturing and control.
Unlike any other information source, gmp review is dedicated to helping you understand and keep up with the often complex and jargon-ridden regulations which are being introduced all the time from Brussels, the FDA and other agencies.

Learn more    
Cleanroom Management in Pharmaceuticals and Healthcare Everything you need to know about the operation and management of cleanrooms. In 26 Chapters and over 600 pages this book provides a unique tool to help you achieve regulatory compliance.

Learn more

ad4

Books

Books of pharmaceutical and medical interest.
 

Learn More

ad5

Journals

Range of journals of interest to scientists and technologists in the pharmaceutical industry.

Learn More

PharmacoVigilance Review

PVR-cover

PharmacoVigilance Review

Editor - Rob Begnett with an advisory panel of Mauricha Marcussen, David Cousins, Graeme Ladds and Sunayana Shah

A Quarterly journal researched and edited by an expert team experienced in all aspects of the safe use of medicines and medical devices.

PharmacoVigilance Review, is dedicated to the analysis of international regulations and informed comment on drug safety issues.

Subscribe Now and you can be confident that you will be better informed on the regulatory interpretation of pharmacovigilance and the safe use of medicines and medical devices than ever before.

ISSN 1752-6752

Contents include:

  • Review of the new role of the European Qualified Person
  • Comparison of EU and US regulations
  • Examination of the demands of pharmacovigilance inspections
  • Understanding new guidelines on the Periodic Safety Updates Reports (PSUR)
  • Debate on the effects of the Clinical Trials Directive
  • Interpretation of the FDA's Risk Management Guidance
  • Report on EMEA guideline on pharmacovigilance for paediatric medicines
  • Discussion on the challenges of medical device vigilance
  • Evaluation of the effects of Volume 9A on all matters of drug safety

 

ico pdf  Content PV Vol5 No1.pdf

ico pdf  Content PV Vol5 No2.pdf

ico pdf  Content PV Vol5 No3.pdf

ico pdf  Content PV Vol5 No4.pdf

ico pdf  Content PV Vol6 No1.pdf

ico pdf  Content PV Vol6 No2.pdf

ico pdf  Content PV Vol6 No3.pdf

ico pdf  Content PV Vol6 No4.pdf

ico pdf  Content PV Vol7 No1.pdf

 

Order now
Product
342
PharmacoVigilance Review
Price/Unit
£ 175.00
Qty
DeliveryCosts