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If you are associated with pharmaceutical profession i.e. quality control, quality assurance, regulatory affairs or pharmaceutical production then you need to know about recent updates about pharmaceutical guidelines. We provide you these updates about cGMP, WHO, USFDA, ICH, MCC, TGA, MCA, MHRA, Schedule M, clinical trials and all other regulatory pharma guidelines. It will help to all pharmaceutical professionals and freshers who want to enter in pharmaceutical profession. Freshers will also get calibration of all instruments and equipments and other useful information. We regularly write over this site on all pharmaceutical topics on Pharma Manufacturing, Quality Control, Quality assurance and regulatory affairs. We also cover the pharmaceutical validations and qualifications, Pharmaceutical Manufacturing SOPs and Current Good Manufacturing Practices in pharmaceutical production. So, this site
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Rajarshi N. Patel
If you are associated with pharmaceutical profession i.e. quality control, quality assurance, regulatory affairs or pharmaceutical production then you need to know about recent updates about pharmaceutical guidelines. We provide you these updates about cGMP, WHO, USFDA, ICH, MCC, TGA, MCA, MHRA, Schedule M, clinical trials and all other regulatory pharma guidelines. It will help to all pharmaceutical professionals and freshers who want to enter in pharmaceutical profession. Freshers will also get calibration of all instruments and equipments and other useful information. We regularly write over this site on all pharmaceutical topics on Pharma Manufacturing, Quality Control, Quality assurance and regulatory affairs. We also cover the pharmaceutical validations and qualifications, Pharmaceutical Manufacturing SOPs and Current Good Manufacturing Practices in pharmaceutical production. So, this site
regularly.
Upcomming Articles: FDA regulations clinical trials, FDA validation guidelines, 21 cfr part 11 compliance, GMP compliance, FDA compliance, FDA audit, Pharma manufacturing, Pharma regulatory affairs, Medical device validation, GMP validation, 21 cfr part 820, Regulatory affairs, Clinical trial FDA, HPLC Method Validation, FDA validation, Validation Control, Pharna regulatory compliance, HVAC validation, Pharma water system
Rajarshi N. Patel
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