Know more about Anshu Yadav - Author and Founder of Quallpharma Consultancy
Hello Readers,
Anshu Yadav is a professional blogger having rich experience in regulatory feild like USFDA guidelines, ICH guidelines, WHO guidelines, GMP guidelines, MHRA guidelines, Schedule M and all other regulatory guidelines. She has completed her MSc in Industrial Biotechnology management (Specialization in Quality Hygiene safety and environment) from Lille Catholic University, France and than joined leading FMCG like Cargill India Pvt ltd. and Sharp Mint Limited. She has started blog with the name "QUALLPHARMA CONSULTANCY" to share her knowledge and expertise with the professionnal. A fresher in pharma field can get all latest information about GMP guidelines for QA, QC, Production and Microbiology.
Readers may contact Anshu yadav at quallpharmaconsultancy@gmail.com or anshuyadav.icgian@gmail.com.
About Quallpharma Consultancy
Qualpharma Consultancy provides describe topics such as change control, deviations, market complaints, process validation, cleaning validation cGMP and other pharma documentation and guideline. Qualpharma Consultancy has strived to help readers to adopt new technologies and ensure that changes to your processes are compliant with current Good Manufacturing Practices (cGMP).
Hello Readers,
Anshu Yadav is a professional blogger having rich experience in regulatory feild like USFDA guidelines, ICH guidelines, WHO guidelines, GMP guidelines, MHRA guidelines, Schedule M and all other regulatory guidelines. She has completed her MSc in Industrial Biotechnology management (Specialization in Quality Hygiene safety and environment) from Lille Catholic University, France and than joined leading FMCG like Cargill India Pvt ltd. and Sharp Mint Limited. She has started blog with the name "QUALLPHARMA CONSULTANCY" to share her knowledge and expertise with the professionnal. A fresher in pharma field can get all latest information about GMP guidelines for QA, QC, Production and Microbiology.
Readers may contact Anshu yadav at quallpharmaconsultancy@gmail.com or anshuyadav.icgian@gmail.com.
Qualpharma Consultancy provides describe topics such as change control, deviations, market complaints, process validation, cleaning validation cGMP and other pharma documentation and guideline. Qualpharma Consultancy has strived to help readers to adopt new technologies and ensure that changes to your processes are compliant with current Good Manufacturing Practices (cGMP).
