Certificate in GMP (Indian Perspective)

Pharmaceutical manufacturing units in India produce millions of medicines daily to support the nation’s healthcare system. Ensuring their quality, safety, and efficacy relies on strict adherence to Good Manufacturing Practices (GMP). Under the Drugs and Cosmetics Act, 1940, and Rules, 1945, GMP implementation is governed by the Central Drugs Standard Control Organization (CDSCO) which defines the requirements for premises, equipment, personnel, documentation, and manufacturing operations.

GMP compliance assures the integrity, safety, and consistency of pharmaceutical products by emphasizing quality control, validated processes, and risk minimization throughout production. It builds confidence in the reliability of medicines and ensures they meet regulatory standards. Aligning with WHO-GMP and PIC/S norms, CDSCO’s GMP framework also enhances India’s global credibility, supporting export quality and patient safety. Thus, GMP under the Indian perspective safeguards public health and reinforces India’s position as a trusted global pharmaceutical manufacturer.

This program will enable the participants to:

• Understand the principles and importance of Good Manufacturing Practices (GMP) from the Indian regulatory perspective.
• Gain knowledge of CDSCO regulations and the requirements of Schedule M under the Drugs and Cosmetics Act and Rules.
• Learn how GMP ensures the quality, safety, and efficacy of pharmaceutical products.
• Develop the ability to implement quality assurance systems, documentation practices, and process controls in compliance with Indian GMP.
• Recognize the role of GMP in regulatory compliance, risk management, and global market acceptance.
• Appreciate the significance of harmonization with WHO-GMP and PIC/S standards for international credibility.
• Apply GMP principles to maintain product integrity, minimize errors, and promote continuous quality improvement within manufacturing facilities.

Target Audience

The Certificate Program in GMP – Indian Perspective (CDSCO) is designed for professionals and students seeking to build or enhance their expertise in pharmaceutical manufacturing and regulatory compliance within India. It is ideal for:

• Pharmaceutical manufacturing professionals involved in production, quality assurance, and quality control.
• Regulatory affairs executives aiming to understand CDSCO and Schedule M requirements.
• R&D and validation specialists seeking to align laboratory and process practices with GMP standards.
• Auditors and compliance officers responsible for ensuring adherence to Indian GMP regulations.
• Academicians and postgraduate students in pharmacy, life sciences, and biotechnology aspiring to enter the pharmaceutical quality sector.

Certified Study Resources

Module 1: Introduction to GMP and Regulatory Framework in India

Module 2: Schedule M – GMP Requirements for Premises, Plant, and Equipment

Module 3: Documentation, Records, and Data Integrity

Module 4: Quality Assurance, Quality Control, and Validation

Module 5: Risk Management, Deviations, and CAPA System

Module 6: GMP Inspection, Compliance, and Global Harmonization

Module 7: Capstone Project

Eligibility

Graduates in any discipline are eligible for our Post Graduate Diploma, Executive Diploma and Professional Certification Programmes.

Programme Duration

The duration of the training is 5 days

Programme Mode

Registration is currently open for Part-time (Online Live Classes) mode.

Programme Deliverables

The accompanying training is appropriately aligned with the current Industry’s expectations.

• Interactive or online live sessions on all key areas of the programme giving all flexibility to the participants.
• All the efforts are made by IGMPI faculty members to make the entire programme modules easily understandable.
• Assessment and evaluation for all the programme modules in order to enhance the levels of competencies and skills of the participants leading towards the objective of application in the job.
• At the end of each programme modules, the trainers shall obtain feedback from the participants using specially designed questionnaires.
• All learning and training delivery initiatives shall be conducted in English.

Assessment & Certification

All the participants are expected to appear for online assessment. After successfully qualifying the examination, the participants will be awarded Certificate in GMP (Indian Perspective) by Faculty of Pharmaceutical Sciences, IGMPI.

Placement Assistance & Corporate Relations

The Institute has partnered with many organizations for providing placement assistance to its participants. The robust placement cell comprises of senior level Human Resources professionals and Talent Acquisition experts which maintains close links with business and industry. We are engaged in promoting the employability of our participants by maintaining good rapport and relation with HR cell and recruiting managers of leading food and agriculture companies across the globe. The efforts of our placement cell also include helping with professional resume writing, interview skills & conducting mock interviews etc.

In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare like Dr. Reddy's Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, IPCA Laboratories, Calyx, Bliss GVS Pharma, SeQuent, Mankind, Beryl Drugs, Allergy Therapeutics, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy , Biocon etc. The IGMPI's Corporate Resource Division actively recommends our students and training participants for various job requirements and specialized roles to Human Resource, Talent Acquisition as well as the heads of various departments in Pharmaceutical, Healthcare industries on regular basis.

Future Prospects

The future prospects for professionals certified in Good Manufacturing Practices (GMP) from the Indian (CDSCO) perspective are highly promising. With India’s pharmaceutical industry expanding globally and aligning its GMP standards with WHO-GMP and PIC/S norms, there is a growing demand for skilled professionals who can ensure compliance, quality, and regulatory integrity. Certified individuals can pursue careers in pharmaceutical manufacturing, quality assurance, quality control, regulatory affairs, validation, and auditing. As CDSCO implements revised Schedule M requirements and strengthens inspection mechanisms, trained GMP professionals will play a crucial role in maintaining India’s reputation as a trusted global supplier of high-quality medicines. This certification not only enhances employability and international credibility but also opens pathways for advanced roles in compliance management, regulatory consulting, and global quality leadership.

GMP professionals are seen in all different types of domain which include QA GMP Manager, Manufacturing chemist, Warehouse Manager, Pharmaceutical GMP Administrator, Data Integrity Specialist and many more in reputed companies.

View Prospectus

Apply Online

Last date for submitting completed Application Form: 11:59 PM 16^th Oct 2025.

For further enquiries, call or write to us on:
18001031071 (Toll Free -9:00 am to 5:30 pm IST-except on Central Government holidays)/ info@igmpi.ac.in