The Pharma Legal Handbook: Europe
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The Pharma Legal Handbook: Europe contains 19 comprehensive country legal guides and answers essential questions about the legal and regulatory environment for pharmaceutical companies in Europe. It is a must-have for any company operating in the continent or looking to enter the market.
Countries featured:
Baltics, Belgium, Bulgaria, Croatia, Czech Republic, Denmark, Germany, Greece, Ireland, Italy, Luxembourg, Portugal, Romania, Russia, Slovakia, Spain, Switzerland, Ukraine and United Kingdom
Prepared in association with some of the continent's leading law firms, The Pharma Legal Handbook: Europe should answer any questions linked to regulation, pricing, clinical and preclinical trials, marketing, manufacturing, trademarks and patents, cannabinoid medicines, medical cannabis and opioid drugs.
About
1. Regulatory, Pricing, and Reimbursement Overview
2. Preclinical & Clinical Trial Requirements
3. Marketing, Manufacturing, Packaging & Labeling, Advertising
4. Traditional Medicines and Over-the-Counter Products
5. Product Liability
6. Patents and Trademarks
7. Regulatory Reforms
8. Cannabinoid Drugs
9. Medical Cannabis
10. Opioid Drugs
11. Orphan Drugs & Rare Diseases
12. Localization
13. Biosimilars & Biologics