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cGMP

cGMP is indicating a current good manufacturing practice of industry.

Impurities in Drug Substances as per IP in pharma

impurities-in-drug-substances

Impurities In Drug Substances: Impurities fall into one or more of the following categories: Inorganic Impurities Organic Impurities Residual solvent Inorganic Impurities in drug substances: …

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Good Documentation Practices Dos and Donts

Good Documentation practices does and donts 1

Good Documentation Practices Dos and Donts (GDP): Good Documentation Practices (GDP) Do’s: Use the defined colored ball pen for document entry. Use the defined date …

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What is form 482-483 and 484 in pharma?

Generally, this question comes to mind of every pharma person working in the industry. So, what is the exact meaning of these forms lets understand …

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50 Pharmaceutical laboratory equipment list / Instrument list

Pharmaceutical Laboratory Equipment List In pharmaceutical laboratories what are the equipment or instrument are used that helps to generates the results. Here is the pharmaceutical …

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Top 10 reason for getting Warning letter to employees

Not only in the pharmaceutical industry but all industries having a root of a treat for not following the company rules and policies. There is …

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Best 24 Definition of Pharmaceutical Terms and dosage forms

In pharmaceutical industry multiple terminology are being used.Here we will understand definition of pharmaceutical terms and dosage forms. Pharmaceutical industry is a manufacturer of multiple …

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Current Good Manufacturing Practices (cGMP) 10 principle’s

Good Manufacturing Practices (GMP) is a set of guidance, regulation, and codes. GMP is also known as Current Good Manufacturing Practices (cGMP).To get consistent and quality …

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Impact of Contamination, cross-contamination & mix-ups in Pharmaceutical

Contamination, crosscontamination and mix-ups is big challenge for pharmaceutical industry. To avoid contamination and mix-ups precautions need to take.

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