Pharmaceutics and Drug Safety

Intellectual property rights and regulatory issues

Regulatory affairs is a field that keeps an eye on how foods, medications, and medical devices are created, tested, produced, marketed, and distributed to make sure they adhere to regulations for human consumption. Experts in regulatory affairs are responsible to make sure that manufacturers follow all applicable laws and regulations at the every stage of product development. Regulatory affairs are understood in a very specific way in the healthcare sector. Pharmaceuticals that are high-quality, safe, and effective are produced and distributed in accordance with its regulations. With the adoption of new rules and technological advancements, pharmaceutical formulation must now contend with new objectives and challenges.

Regulations, guidelines, and technologies

• GMP
• CGMP