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Important Difference between 21 CFR part 11 and EU Annex 11

by Pharmabeej

21 CFR part 11 and EU annex 11 both are guidance for the electronic records and electronic signature. The guidances are applied to the computerized systems that used to store the electronic data. FDA has …

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Friability test: Top 18 Friability test Interview Question and Answer

by Pharmabeej

A Good Interview is a first and last impression on the interviewer. More you know more you fearless while interview. It is more important to be knowledgeable in the industry to show our existence for …

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Best 24 Definition of Pharmaceutical Terms and dosage forms

by Pharmabeej

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 dosage forms like as Solid oral, Liquid oral, Nasal spray, …

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31 most important interview questions and answers on dissolution for quality control in pharma

by Pharmabeej

How to face interview is quite difficult problem for newbie.In this article I tried to cover top interview questions and answers on dissolution. Most common interview questions and answers on dissolution that helps to candidate …

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What are 3 Practical Difference between assay potency and purity in Pharmaceutical?

by Pharmabeej

The difference between assay potency and purity in pharmaceutical industry. Assay can be calculated by three different ways. Such as assay on dried basis, assay on anhydrous basis and assay on as us basis.

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Understand 14 ICH guidelines in the pharmaceutical in an easy way

by Pharmabeej

ICH full form: International Council on Harmonisation of a technical requirement for registration of pharmaceutical for human use.  ICH is a joint initiative of three different regulatory bodies (USA, Europe, and Japan) as per their region to discuss …

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10 Principle of Quality Control instruments in pharma lab

by Pharmabeej

Principle of Quality control instruments in Pharma lab In the pharmaceutical industry, multiple instruments are used. In this article, we are going to explain the Principles of Quality Control instruments in the pharma lab.   In …

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Important 4 Difference Between Dissolution and Disintegration test in pharmaceutical

by Pharmabeej

      In the pharmaceutical industry, difference between Dissolution and Disintegration is quite difficult to understand for the newbies. These terms are look like as a same but both are having different mechanism to perform …

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What is Drug Master File (DMF) and types of Drug master file in pharmaceutical

by Pharmabeej

Drug Master File (DMF) is a confidential data provided by the manufacturer to the Food and Drug Administration (FDA) for review, before approving any product to market in the United States of America (USA). In …

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Best basic information of Particle size analysis (PSD)

by Pharmabeej

Particle size analysis is an analytical technique to measure and report the distribution of particle size of solid or liquid material. Particle size analysis   Disturbance of particle size can impact the flow property of …

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  • Bharat serums and vaccines ltd opening for RA-apply now
  • 50 Electronic Codes of Federal Regulation (e-CFR) in pharma
  • Pulse Pharma Openings for Production / R&D / FR&D / AR&D / Nano R&D department-Apply Now
  • Neuland Laboratories Ltd Walk-in-interview on 27th Feb 2021 for multiple positions
  • Elixir phrma Urgent opening for multiple dept – Apply Now

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