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A presentation on introduction of calibration, qualification and validation in pharmaceutical indust...
overview of dossier
Pharmaceutical validation for manufacure of quality products and documentation.
This presentation contain introduction to Good Distribution Practices Guideline. and Legal GDP requi...
Regulatory perspective of clinical trials, phases of clinical trials,ICH-GCP Principles
Q.R are planned and documented by an inspections of a review item The review item may be a product,...
In this slide contains SITE ACCEPTANCE TEST IN QUALIFICATION. Presented by: K. SANDHYA RANI (Depart...
Personnel Section about the Current Good Manufacturing Practice
Bioethics and its principle and its difference with healthcare ethics
Data integrity: Definition, data integrity principles, examples, warning letters , implementation
A short note on Quality Management of Hospital Services for Public Health students at Post Graduate ...
a case study presentation on physiotherapy management of knee osteoarthritis
OBJECTIVES AIM ICH ORGANISATION STRUCTURE ICH MEMBERS ICH VARIOUS GUIDELINES ICH GUIDELINES CATEGORI...
FOR PHARMA FRANCHISE IN YOUR AREA: CONTACT: +91-9041677932 Trumac Healthcare is leading manufactu...
In this topic , it covers about standard operating procedure in pharmaceutical quality assurance. t...
A brief review on ISO 14644 Standard on Cleanroom Design and testings. With a look at PIC/S and WHO ...
regulation
Materiovigilance, Medical device safety, and MvPI (Materiovigilance Programme of India)
Good clinical practices-drug discovery
Standard Operating procedure(SOP), Preparation review ,Approval Issuance of master batch Record MBR ...
Manufacturing of aspirin with respect to processes in industry
Good clinical practice ICH GCP E6
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Auditing a vendor is truly an essential part of QMS. This presentation describes the terminologies u...