Customizing trainings for US based Medical Device Company on GLP, Proficiency Testing Programs, OECD guidelines Trainings, CAPA verification. Quality Culture, How to Prevent Human Errors.
Conducting Mock Audits
Training on Do’s and Don’t during inspections
Participated in conferences on Computer System Validations and Data Integrity as an expert.
Providing trainings to BPharma/Mpharma Students on Pharmaceutical Quality System, Quality Metrics, data Integrity
I am also conducting training at NIPER sponsored by the followings :
– Govt of India , Ministry of External Affairs under the Indian Technical and Economic Cooperation under Ministry of Health for ITEC on , QbD, Analytical Method Validation, Quality Assurance and Quality Control etc
For Small and Medium Pharmaceutical Industry Topics Technology Transfer, QA and QC, Pharmaceutical Quality System.
Handling Project of Pharmaceuticals company, for conducting Quality audits of Beta Lactam, Non Beta Lactam Sterile facilities, Nutraceuticals and OSD manufacturers
Conducted two days extensive training for Medical device companies on 21 CFR Part 58, ISO 17025 requirements, Computer System Validation and regulations on Electronic records and Electronic signatures ( 21 CFR Part 11).