How to Utilize 5 WHY Analysis to Uncover Root Cause
5 Whys analysis is an essential tool for identifying the root causes of issues in the pharmaceutical industry
Pharma Interview
23 articles tagged “Pharma Interview”
Departments in the Biopharmaceutical Industry
Departments in biopharmaceutical industry, its work function in details, how to get job in biopharmaceuticals, eligibility criteria, Salary.
How to Secure a Job in the Pharmaceutical Industry: Eligibility, Preparation, and Interview Tips
Its essential to not only meet the eligibility criteria but also to showcase your passion for the industry & willingness to learn and grow.
Biophore India Pharmaceuticals Pvt. Ltd. Walk-In Interview On 30 March to 1 April 2023
Biophore India Pharmaceuticals Pvt. Ltd. Walk-In Interview On 30th March to 1 April 2023
Sun Pharma- Walk-In Interview On 31-MAR-23
Sun Pharma- Walk-In Interview On 31-MAR-23
Teva Pharmaceuticals Hiring Clinical Research team for Bangalore/ Mumbai location
Teva Pharmaceuticals Hiring Clinical Research team for Bangalore/ Mumbai location.
Nectar Lifesciences Limited, Walk-In Interview on 09-APR-23
Nectar Lifesciences Limited, Walk-In Interview for Derabassi Plant on 09-APR-23 at HOTEL WINWAY, 164/1, RNT MARG, INDORE
Water for Hemodialysis
Water for Hemodialysis is used for hemodialysis applications, primarily the dilution of hemodialysis concentrate solutions.
Purified Water [PW]
PW is used as an excipient in the production of nonparenteral preparations & in other pharma applications, such as cleaning of equipment.
Installation Qualification [IQ]
The performance of tests to ensure that the system etc. used in a manufacturing process are appropriately selected and correctly installed.
What is Difference between Quality Control and Quality Assurance?
What is Difference between Quality Control and Quality Assurance?
0.1N & 0.1M HCl Preparation: Formula + Calculation Guide
How to calculate the requirement of commercially available Concentrated Hydrochloric Acid to prepare 0.1N or 0.1M HCl Solution?
SOPs in Pharmaceuticals: Format, Structure & Writing Guide
Standard operating procedures (SOPs) are the detailed written instructions that specify how a test or administrative procedure is to be performed, or how a piece of equipment is operated, maintained and calibrated. SOPs describe the \"standard\" approved procedures that are routinely carried out in a GMP facility. They indicate exactly how things are done and are kept current by review and approved revision on a predetermined schedule
Films PHARMACEUTICAL DOSAGE FORMS
USP-43 〈1151〉 Films PHARMACEUTICAL DOSAGE FORMS
Capsules PHARMACEUTICAL DOSAGE FORMS
Capsules PHARMACEUTICAL DOSAGE FORMS, United State Pharmacopoeia USP-43, Chapter <1151>
Aerosol Dosage Forms: Types, Formulation & Examples
Aerosols PHARMACEUTICAL DOSAGE FORMS, United State Pharmacopoeia USP-43
Parenteral Dosage Forms: Types, Requirements & Examples
INJECTIONS AND IMPLANTED DRUG PRODUCTS (PARENTERALS)—PRODUCT QUALITY TESTS This article is based on the requirement of the United State Pharmacopoeia…
INSPECTION OF UTILITIES
Co-operation Scheme (PIC/S) has revised the guidance document for INSPECTION OF UTILITIES on 19 January 2021
QRM Implementation: PIC/S Aide-Mémoire & Assessment Guide
Pharmaceutical Inspection Co-operation Scheme (PIC/S) Leading the international development, implementation, and maintenance of harmonized GMP standards…
Site Master File (SMF): WHO Format, Contents & Example
In this article, we will discuss a practical approach to prepare the Site Master File (SMF) for the Pharmaceutical Industry. We have to understand that The SMF is the document which explains your organization; it creates the image of the organization, So it should be self-explanatory as in most of the case you are not present to explain the SMF.Do you believe that the SMF is creating the first impression of your organization before visiting your Site…After discussing with various regulatory auth
Pharmaceutical Documentation: Hierarchy, Types & GMP Rules
You might have read so many guidelines and articles on Documentation, in this article, I am not going to explain the same things here.
Quality Policy for Pharmaceutical Industry
In this article, we will learn about Quality Policy In the pharmaceutical industry Quality Policy is classified as a level-1 document Importance…
JOB in Pharma
Pharmaceutical Industry contributes to improving the health and wellbeing of society.