Path For Process Management
It shows the relationship among management processes, operational processes & support processes , ultimately affecting on patients & health institutions. For any feedback or suggestions…
Quality Assurance
Introduction : “Quality Assurance” is the sum total of the organized arrangements made with the object of ensuring that all drug substances & drug products…
History of Indian Pharma Industry
The History of Indian Pharma Industry – Part 1 focuses on the Indian pharma industry growth story of India’s pre-independence era. With Dr. PC Ray…
Vendor Qualification (VQ)
VQ: Vendor qualification is the process by which a vendor is evaluated to determine if it can provide the necessary goods or services to the standards…
Analytical Method Transfer (AMT)
AMT : It is the Documented process that qualifies a laboratory (receiving laboratory) to use an analytical method that originated in another laboratory (transferring laboratory), whether that is internal…
Validation of New Process
Process validation is the collection and evaluation of data, from the process design stage throughout production, which establishes scientific evidence that a process is capable of consistently delivering quality products.
USFDA: List of Off-Patent, Off-Exclusivity Drugs without an Approved Generic
Current List of Off-Patent, Off-Exclusivity Drugs without an Approved Generic Find here and keep yourself updated on a list maintained by FDA of approved new…
Sampling tools
Scoops / Spatula Small containers of solid materials may be adequately sampled using a spatula or scoop. The samples are then blended to provide a…
Near Miss Report
Near Miss is an unplanned event that did not result in an injury or property damage, but had the potential to do so.
Bar code
What is Barcoding? The small image of lines, or bars, and spaces are affixed to nearly everything you can imagine, for identification purposes. Specifically, barcodes use a…
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