In this section you will find information products, including market research, covering regulatory issues concerning the global biotechnology & pharmaceutical industries, including Good Laboratory & Clinical Practice (GLP & GCP), pricing & reimbursement and drug approval in Europe, the US and Asia.

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Title	Publication Date	Price
IMS Pharmaceutical Pricing & Reimbursement Concise Guide: UK	December 2011	£420
Drug Recalls and Warning Letters Increasing Numbers Caused by Manufacturing Errors and Regulatory Non-Compliance Issues	November 2011	£2215
Pharmacovigilance and Other Pharma Regulatory Developments 2011 - 2021	August 2011	£1499
Pharmacovigilance and Related Developments 2011-2021	August 2011	£1499
MSL-KOL Engagement Ensuring Compliance	June 2011	£335
India Pharmaceutical Regulatory Report 2011 (Report Only)	April 2011	£475
Chinese Pharmaceutical Regulatory Report 2011 (with Appendix)	April 2011	£1010
Martindale: The Complete Drug Reference 37th edition	April 2011	£399.99
Impact of Healthcare Reforms on the Medical Technology Industry	March 2011	£4110
Latest Chinese Regulations for Imported Drug Registration China Pharmaceutical Guidebook	February 2011	£945
Reforms to the Pharmaceutical Benefits Scheme in Australia	February 2011	£315
A Guidebook of Registration Application for Imported Chemical Drugs China Pharmaceutical Guidebook Series (2) (3rd edition) Material and Clinical Trial Requirements of Application and Approval for Imported Drug Registration	February 2011	£475
A Comprehensive Guidebook for Foreign Pharmaceutical Companies China Pharmaceutical Guidebook Series (1) (3rd edition) Latest Chinese Regulations for Imported Drug Registration	February 2011	£475
The Dietary Supplements Regulatory and Market Outlook	February 2011	£3030
A Guidebook of Registration Application for Imported Traditional Chinese Medicines and Natural Medicines China Pharmaceutical Guidebook Series (3) (3rd edition) Material and Clinical Trial Requirements of Application and Approval for Imported Drug Registration	February 2011	£475
A Guidebook of Registration Application for Imported Biological Products China Pharmaceutical Guidebook Series (4) (3rd edition) Material and Clinical Trial Requirements of Application and Approval for Imported Drug Registration	February 2011	£475
Biosimilars Regulatory Update an evolving landscape	February 2011	£295
US Regulatory Trends During 2010 A Rapidly Changing Environment	January 2011	£305
Obama's Healthcare Reform Bill and its Impact on the U.S. Healthcare Market	August 2010	£2940
Healthcare Reform 2010 Medical Device Industry Perceptions Survey	August 2010	£6325
Pricing & Reimbursement in Emerging Markets Analysis of pricing mechanisms and the influence of public and private sector health insurance provision	August 2010	£2425
Pay-for-Delay An Unsettled Future Lies Ahead	July 2010	£295
The Impact of Healthcare Reform on Revenue Management Unsettled and Uncertain	June 2010	£950
Pricing and Reimbursement Strategies for Diagnostics Overcoming reimbursement issues and navigating the regulatory environment	June 2010	£2425
US Healthcare Reform Impact and Implications for the Pharmaceutical and Biotech Industries	May 2010	£220
Royalty Financing Terms and Agreements in Pharma, Biotech and Diagnostics 2nd edition	May 2010	£1705
Healthcare Reform Impact on Medical Device Industry	April 2010	£315
Japan Compliance Environmental, Health, and Safety Management Trends 2009	February 2010	£3160
Business Strategy: Healthcare Reform Impact on Healthcare Payer Business and Technology Priorities in the 2010 Decade	January 2010	£2845
Pharmas Seek FDA Guidance on Social Media	November 2009	£950

Results 1 - 30 of 56
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