This Certificate Programme has been designed to help manufacturers gain awareness of quality requirements regarding validation and the nature of “special processes”. This programme targets Quality, Product Development and Manufacturing personnel involved in process validation, Regulatory Affairs Managers and auditors of manufacturing firms (internal and external).
This certificate reduce development time with better understanding of validation, faster market access with more compliant products, Increase sales and customer satisfaction with professional development and knowledge sharing. The validation programme is ideal for anyone in the Pharmaceutical, Medical Device, Biotech, Biopharmaceutical and Skin/Cosmetic industries who is tasked with validation.
The case study based approach in certificate programme is designed for working professionals in full time employment who want to update their knowledge and gain required skills and attitude in the area in order to become a certified GMP professional in the domain. This certificate is also beneficial for professionals from different streams to help them intensify their knowledge. This is an advanced certificate having rigorous case studies based methodology throughout the duration.
Module 1 : Quality, Quality Assurance and Quality Control in Pharmaceutical
Module 2 : Introduction to Validation and Types
Module 3 : Process Validation
Module 4 : Cleaning Validation
Module 5 : Method Validation
Module 6 : Equipment and Facility Validation
Module 7 : Computer System Validation
Module 8 : Qualification and Validation(FDA and WHO perspectives)
Module 9 : Quality Control checks, Inspections and Audits
Module 10 : Government Regulations and Certifications, ICH guidelines, ISO 9000 and 9001
Any graduation/ B.tech/ B.Sc. in Microbiology/ Life Sciences/ Botany/ Zoology/ Food Science/ Food Technology/ BE/ B.Pharma/ MBBS/ BDS/ BHMS/ BUMS/ BAMS or any other discipline. Diploma holders are eligible for our Executive Diploma, Industry Certificate, and Certificate Programmes.
Minimum duration to complete this programme is 3 months and maximum is 6 months.
The registration dates for this programme run by the Institute are updated timely on the webpage. Effective Online learning tools incorporated into the design of the webpage make the Programme lectures, online live classes and study material easily accessible. This gives a huge window of self-regulated and self-paced performance to the participants.
A comprehensive study material for all the modules in hard copies ensuring the needs of the audience. The accompanying training material is appropriately aligned with the current Industry’s expectations.
IGMPI follows a credit system based on all learning activities involved in studying for all PG Diploma, Executive Diploma and Certificate Programmes. Each of your modules is equal to 4 credits. To successfully complete the programme, you will have to earn all the credits assigned to your programme.
All the participants are expected to appear for online exam and are also obliged to submit assignments after each module. After successful completion the participants will be awarded Certificate in Pharmaceutical Validation by IGMPI. For all the above mentioned modules elaborate Programme material, assignment and case studies would be provided by the Institute from time to time. Details get updated on the webpage as well.
The Institute has partnered with many organizations for providing with placement assistance to in its participants. Besides, it has a robust placement cell comprised of senior level Human Resources professionals and Talent Acquisition experts which maintains close links with business and industry. This cell is continuously engaged in promoting the employability of our participants and encouraging the concerned Human Resources department and Hiring Managers to recruit/hire our participants for their vacant positions. The efforts of our placement cell also include helping with professional resume writing & interview skills.
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.
This Programme is relevant to individuals working throughout the pharmaceutical product lifecycle in development, manufacturing, quality, and many other roles involved in validation of products and processes. It will help them to integrate and link the science and risk-based lifecycle approach for Validation to your Pharmaceutical Quality System. Validation professionals evaluate and calibrate the equipment and procedures used in development and production of a variety of products. They ensure all systems are running according to necessary specifications and operate within regulations to ensure the production of quality products.
Pharmaceuticals | Food | Clinical Research | Healthcare | Medical Coding | Medical Device | Nanotechnology | IPR
Featured Article
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI (Building FR&D Talent in India)
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
GMP: A continous process
Fighting fakes with technology
Trends in lab design
Oral solid dosage forms: Trends and opportunities
Optimising FR&D to expedite regulatory complaince
By Shri Vinod Arora, Principal Advisor, IGMPI
Featured Article
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI (Building FR&D Talent in India)
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
Moderated by Shri Vinod Arora, Principal Advisor, IGMPI
GMP: A continous process
Fighting fakes with technology
Trends in lab design
Oral solid dosage forms: Trends and opportunities
Optimising FR&D to expedite regulatory complaince
By Shri Vinod Arora, Principal Advisor, IGMPI
Placement testimonials: Our alumni are working with Fortune 500 and global Pharmaceutical, Food and healthcare giants like