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M. Pharmacy - Pharmaceutical Regulatory Affairs (MRA) 1st Semester - Regulations and Legislation for...
Pharmacovigilance, derived from the Greek words "pharmakon" (drug) and "vigilare"...
The ICH E7 guideline, titled Studies in Support of Special Populations: Geriatrics, provides recomme...
The document filing for a pharmaceutical product is done in the form of dossier. The slides explain ...
Format and contents of dossier filing
The most important aspect for selection of a drug and establishment of the proper pediatric dosage i...
Professional certification can provide added credentials for those who look for greater career succe...
Setting of specification limits as per ICH Q6A
Requirements And Guidelines For Permission To Import / or Manufacture of New Drugs For Sale or To Un...
post traumatic epilepsy
Regulatory Affairs, Responsibilities of Regulatory Affairs Professionals
Research Methodology and Biostatistic...Declaration of Helsinki
drug regulatory affaris
It discuss about the basic knowledge of Stroke and management.
describe about role of sponsor and CRO on clinical trial process
This presentation explains the stages of drug discovery and the clinical evaluation process. It cove...
advanced pharmaceutics
AORTOPATHY
The presentation is about documentation in the pharmaceutical industry. Many important topics are co...
Defination of validation, types of validation.
In bioequivalence studies, the plasma concentration time curve is generally used to assess the rate ...
A typical quality executive job description be included elements such as: quality executive duties, ...
