Scientific Sessions

Regulatory Affairs and Quality Assurance ensure that pharmaceutical products comply with all legal, safety, and quality standards throughout development, manufacturing, and distribution. Regulatory affairs focus on obtaining approvals from authorities and maintaining compliance, while quality assurance guarantees consistent product quality, safety, and efficacy. Together, they uphold patient safety, efficacy, and trust in healthcare products. Topics related to Good Manufacturing Practices (GMP), stability testing, bioequivalence, and document submission to global regulatory agencies like FDA, EMA, and ICH. Effective regulatory planning accelerates approvals and minimizes development risks.