Courses

Short Course Program

To equip learners with essential knowledge and practical skills in regulatory affairs, enabling them to understand industry requirements and confidently perform entry-level regulatory tasks in the pharmaceutical and healthcare sectors.

The Short Course Program is an intensive, one-month training designed to provide a solid foundation in Regulatory Affairs for individuals who want to quickly develop job-ready skills. This program is ideal for both registered pharmacists seeking to expand their expertise and non-pharmacists aspiring to enter the pharmaceutical or healthcare industry.

Throughout the course, participants will gain an in-depth understanding of the regulatory processes governing the registration, approval, and post-marketing compliance of pharmaceutical products in the Philippines. The curriculum includes practical lessons on FDA submission requirements, product dossier preparation, labeling compliance, Good Manufacturing Practices (GMP), and local and international regulations.

Each session is guided by experienced regulatory professionals who share real-world applications, case studies, and current industry trends to bridge theory and practice. Learners will also engage in hands-on exercises, mock regulatory document preparation, and simulated evaluations that mirror actual workplace responsibilities.

With flexible daytime schedules and a focused learning approach, the Short Course allows participants to balance study and work commitments while still gaining comprehensive exposure to the regulatory landscape. By the end of the program, graduates will have a clear understanding of the regulatory workflow, enhanced documentation skills, and the confidence to pursue entry-level roles in regulatory affairs or compliance departments.

Traditional Course

To provide an in-depth and structured understanding of regulatory affairs, preparing learners to handle complex documentation, compliance processes, and regulatory submissions with confidence and competence in both local and international settings.

The Traditional Course Program is a comprehensive three-month training designed for individuals who want to develop a deeper, more thorough understanding of Regulatory Affairs. It caters to both pharmacists and non-pharmacists who aim to build a long-term career in the pharmaceutical, medical device, or healthcare industries.

This program goes beyond the basics, offering extensive coverage of regulatory concepts, policies, and procedures. Students will explore the entire regulatory lifecycle — from product development and registration to post-marketing surveillance and compliance. Topics include Good Regulatory Practice (GRP), Good Distribution Practice (GDP), pharmaceutical product dossier compilation, labeling and packaging regulations, clinical trial applications, and pharmacovigilance requirements.

Through interactive lectures, workshops, and case discussions, participants learn how to interpret and apply current FDA and international regulatory standards. The program also emphasizes critical thinking, documentation accuracy, and ethical responsibility — essential qualities for future regulatory professionals.

Learners are guided by experienced mentors who provide personalized instruction and industry insights. Each session includes hands-on exercises such as preparing regulatory documents, conducting mock submissions, and analyzing real-world case studies to simulate actual industry work.

With flexible schedules and progressive pacing, the Traditional Course allows learners to fully absorb each topic while maintaining balance with other commitments. By the end of the program, graduates will have mastered the technical knowledge and professional confidence required to pursue roles such as Regulatory Affairs Associate, Compliance Officer, or Documentation Specialist in the growing field of regulatory affairs.