The white paper on the Future of Tamper-Proof Pharmaceutical Packaging starts with an introductory note on the pharmaceutical industry. It focuses on the falsified medicine, its definition, problems, and its different types. Falsified medicine is the production of counterfeit pharmaceutical products that do not comply with strict regulatory standards imposed by government. The paper discusses the negative impact of this falsification of medicine as well as the existing laws and regulations imposed by the government agencies to prevent the selling of falsified medicine. It also throws light on the new regulations and its applications.
The paper has been prepared to the context of Commission Delegated Regulation (EU) 2016/161, effective 2019.
The paper will be useful to R&D Scientists, Packaging professionals, Health & Regulatory experts in the Pharmaceutical industry.
Credit: Origin Pharma Packaging (www.originltd.com)