Category: Method Development

Pharmaceutical Reference Standards| How to Manage

Pharmaceutical Reference Standards| How to Manage

Pharmaceutical Reference Standards play a vital role in maintaining pharmaceuticals' quality, safety and efficacy at every stage during drug development. In this article, you will learn pharmaceutical reference standards, their types, pharmacopeial standards, applications, advantages and source with FAQs.

Top 11 Pharmaceutical Analytical Techniques Explained

Top 11 Pharmaceutical Analytical Techniques Explained

This article describes the top 11 common pharmaceutical analytical techniques with brief principles, applications and advantages FAQs

Career Opportunities in Pharmaceutical R&D (Research and Development)

Career Opportunities in Pharmaceutical R&D (Research and Development)

This article describes career opportunities in Pharmaceutical R&D, departments, required qualifications, and skills with FAQs

GC Method Adjustments USP Way: What Is The Allowable Limit

GC Method Adjustments USP Way: What Is The Allowable Limit

This article describes GC method adjustments USP way, reasons for failing the SST, and conditions under which adjustments can be made with case studies and FAQs

HPLC Method Adjustment USP Way: What IS The Allowable Limit

HPLC Method Adjustment USP Way: What IS The Allowable Limit

Explore HPLC method adjustment under USP 621 and learn about allowable changes in pharmaceutical analysis for optimal results.

You cannot copy content of this page

×