Risk Management
4 Key Criteria to Consider when Outsourcing Safety Operations in Life Sciences Facilities
September 10 by Jones Lang LaSalleAs life sciences organizations outsource more of their non-core activities, the safety systems associated with those functions become increasingly complex. Managing safety requires a set of capabili...
Advice on the new European GDP guidance
September 03 by Pharmaceuticals & Biotechnology EditorHow will the new GDP guidance affect the clinical supply chain? In particular how will it affect the non IMP supply chain? These guidelines outlined significant changes within the areas of...
6 Game-Changing Tips to Deal with Risk Management & Drug Safety Audit
April 04 by Pharmaceuticals & Biotechnology EditorA Pharmacovigilance audit is important as it ensures the company’s drug safety and risk management procedures comply with applicable laws, regulations and guidance. While it could be a dauntin...
Controversy & Confusion: What Does Annex Z of EN/ISO 14971: 2012 Mean & How Can We Practically Implement It?
December 03 by Helen WinsorChuck Sidebottom, Director, Corporate Standards at Medtronic and Dave Osborn, Manager, International Standards at Philips, join Pharma IQ to discuss the current controversy over the application of ris...
Pharmacovigilance: Pharma Regulatory Compliance Update
September 13 by Niamh MadiganPharmacovigilance is something that has no borders and in July this year, some key regulations were passed which will have a profound effect conceptually and technically on those who...
Pharmacovigilance Brings Drug Safety Beyond Compliance
July 27 by Pharma IQ NewsIQPC’s Pharmacovigilance North America Summit brings together industry experts to address top industry concerns PHILADELPHIA, PA – Pharma IQ, a division of IQPC, announces t...
Can New Media Improve the Output of Pharmacovigilance Data?
May 13 by Shaloo PandhiShaloo Pandhi, Group Head of Pharmacovigilance Operation at Novartis Healthcare, shares his insights on pharmacovigilance in India. Pharma IQ: There is an immense need to address...
Global Drug Safety and Risk Management
May 06 by Elie MagdalaniReported adverse events are an important tool for implementing a risk management program. An important contributing factor in the evolved AEs the condition of chronically ill patients taking a drug da...
Using New Media to Improve the Output of Pharmacovigilance Data
April 05 by Andrea CharlesShaloo Pandhi, Group Head Pharmacovigilance Operation, Novartis Healthcare, India, talks to Andrea Charles from Pharma IQ, about risk management strategies and optimising drug safety activities...
Risk Management for Software Design in Medical Devices from IEC 62304 and ISO 14971 Perspectives
March 31 by Pharma IQ NewsNEW YORK, NY AND SAN DIEGO, CA – (BUSINESSWIRE) –Software quality for safety-critical medical devices has been at the centre of discussion for industry experts and especially the FDA. In...
3 Top Security-Enhancing Tips for Reducing Cargo Thefts
March 15 by Andrea CharlesBarry Tarnef, Assistant Vice President, Senior Loss Control Specialist, Chubb & Son, speaks to Andrea Charles from Pharma IQ, about current risk management trends in the supply chain f...
Three Top Tips for Optimising Physical Form Selection
February 09 by Andrea CharlesWhat strategies are pharmaceutical companies employing to accelerate early development and preformulation? Michael Mitchell, Head of Pharmaceutical Sciences Oss, Merck, speaks to Andrea Charles from...
