regulations
Keeping tabs on pharma: New diabetes treatment for children and DMT studied for stroke patients
February 01 by Leila HawkinsA groundbreaking study shows great promise for children with diabetes, DMT research for stroke patients awaits approval and China tightens anti-monopoly laws
The Boardroom Series: Interview with Orphazyme's CMO Carlos Camozzi Full Interview
June 03 by Pharmaceuticals & Biotechnology EditorDr Carlos Camozzi is the new Chief Medical Officer at the Biotech Company Orphazyme, located in Denmark. Carlos has over 25 years in clinical research and development roles in pharma and biotech com...
Conception to Completion: Why Agile Development for Healthcare?
June 20 by Niamh MadiganAgile methodologies implemented into software development projects in healthcare are fast becoming more popular, but how can you achieve a successful agile project from conception to comp...
Survey: Clinical Trial Supply: Trends & Practices in 2012
April 28 by Pharma IQ SurveysIncreased complexity of clinical trials, entering into new regions, multiple site trials and differing regulatory requirements are all adding to the difficulties of getting the right supplies to t...
European Medicines Agency's Hans-Georg Eichler: Top Priorities to 2015
November 07 by Pharmaceuticals & Biotechnology EditorDr. Hans-Georg Eichler, Senior Medical Officer for the European Medicines Agency, talks to Andrea Charles from Pharma IQ, abut the Agency's growth, starting a common language between p...
High Risk: How Corrupt is Life Sciences?
August 11 by Pharma IQAccording to Transparency International's Bribe Payers Index, among 19 industry sectors globally, life sciences is perceived to be the 6th most corrupt sector, in terms of the propensity of compa...
Roundtable: Best Practices, Skills & Tools to Gain Competitive Edge in Clinical Trials, Part II
May 23 by Alisa Wright, Steven Jacobs, Rafik BisharaThe increasing complexity and globalization of clinical trials has changed the pre-market environment, with more companies outsourcing operations and investigating emerging markets. Pharma IQ hosted...
Roundtable: Best Practices, Skills & Tools to Gain Competitive Edge in Clinical Trials
May 23 by Alisa Wright, Steven Jacobs, Rafik BisharaThe increasing complexity and globalization of clinical trials has changed the pre-market environment, with more companies outsourcing operations and investigating emerging markets. This leads to qu...
Saudi FDA: Working with Industry to Improve the Reporting of Adverse Reactions
May 23 by Dr Nasser Al-QahtaniDr. Nasser Al-Qahtani, Head, Adverse Drug Reactions Evaluations Department, Saudi FDA, joins Pharma IQ to discuss the Saudi FDA’s pharmacovigilance system and what new guidelines he predicts will be a...