What the meaning of value access in pharma?
In the pharmaceutical industry, “Value Access” refers to the strategic process of ensuring that a medicine or healthcare product is not only... Read More
Pharmaceutical Product Management: Skills – You Must Have in 2025
In the fast-evolving world of pharmaceuticals, the role of a Pharmaceutical Product Manager (PPM) has become more critical than ever. With changing... Read More
What is the difference between CMO and CDMO?
Posted on18 Jan 2025
TagsCDMO, CMO, Contract Development and Manufacturing Organization, Contract Manufacturing Organization
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CMOs (Contract Manufacturing Organizations) primarily focus on large-scale manufacturing of drug substances and products, coming into the picture once formulations and processes... Read More
What is cytokine storm?
A cytokine storm is a severe immune reaction in which the body releases an excessive amount of cytokines into the blood too... Read More
What is the meaning of me-too or follow on drugs?
Posted on22 Feb 2024
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Me-too drugs and Follow on drugs are the common terminologies which used by pharmaceutical marketer. A compound that is structurally very similar... Read More
12 Skills what Product Manager should have!
Product managers play a crucial role in driving the success of a product. They need a diverse set of skills to navigate... Read More
What are the difference between Wholesaler and Specialty Pharmacy?
Posted on21 Feb 2024
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There are clear cut difference between the two terms. The wholesalers are the first purchaser of the drug, directly from manufacturer. Specialty... Read More
A case based understanding in co-development deal
Posted on21 Feb 2024
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In a Co-Development Agreement the intellectual property is typically licensed by the licensor to the alliance partner, and as well, the two... Read More
What are the difference between FDA 483 and Warning Letter?
483 observation or FDA 483 and warning letter seems to be same, nut there is difference between the FDA form 483 and... Read More
What is difference between Form 483 and Establishment Investigation Report ?
Form 483 and an Establishment Investigation Report (EIR) are both documents used by regulatory authorities, particularly the U.S. Food and Drug Administration... Read More