Pharma Article

GENERAL PROCEDURE FOR PASSIVATION

07/04/2019

Passivation is a non-electrolytic process to removes free iron from the surface and forms an inert, protective oxide layer that in turn renders the stainless steel more rust-resistance due to lack of iron to react with the atmosphere by using nitric or citric acid. We already discussed about What is Passivation and What are major […]

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How the New Drug approval process of CDSCO works?

03/03/2019

Author: Debarati Bhattacharyya (Kundu) M. Pharm from Jadavpur University. The process of approval of new drug in India is a very intricate process, which should meet necessary requirements. New drug is a medication or therapy that has not been used earlier in clinical practice to treat a disease. A new drug that is marketed after […]

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What is Passivation? How Does Passivation Process Work? How to Passivate Stainless Steel Parts?

13/02/2019

Passivation could be a non-electrolytic method to remove free iron from the surface associated forms an inert, protecting oxide layer that successively renders the stainless-steel a lot of rust-resistance because of lack of iron to react with the atmosphere by using nitric or citric acid. Here we discuss What is Passivation? How Does Passivation Process Work? How to Passivate Stainless Steel Parts? Explore new openings in Pharma Profession […]

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Explore new openings in Pharma Profession by Making yourself Skilled as Technical Associate in The Central Drugs Standard Control Organisation CDSCO

13/02/2019

The Central Drugs Standard Control Organisation (CDSCO) is under Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India and the National Regulatory Authority (NRA) of India. I am disscused here Explore new openings in Pharma profession by making yourself skilled as Technical associate in The Central Drugs Standard Control Organisation (CDSCO). […]

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What is Data Integrity and ALCOA Plus

21/01/2019

Data integrity is key in a pharmaceutical quality system ensuring that products are of the desired quality. Data Integrity is increasingly becoming a critical GMP issue the in the Pharmaceutical and Medical Device Industry. ALCOA-plus. A normally used word form for “attributable, legible, contemporaneous, original and accurate”   The descriptor ALCOA has been around since the 1990’s ensuring by […]

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GOWNING PROCEDURE IN CLEAN ROOM

28/10/2018

GOWNING PROCEDURE IN CLEAN ROOM Most Popular Articles What is the fumigation and fogging? What is viable and nonviable Particle Count? Scope for Science Graduate & Post Graduate Types of Clean Room Airlocks in cGMP Facility Simplified CAPA with Investigation Tools, Route Cause Analysis & Risk Management KNOW ABOUT TOTAL QUALITY MANAGEMENT AND CURRENT GOOD […]

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How to Crack Your Job Interview?

25/10/2018

How to Crack Your Job Interview? Today I shall discuss you a topic which is a very common topic i,e “How to Crack Your Job Interview?” but I can assure you that my experience will reduce the phobia for an interview. First of all, before going for an interview you should decide whether the job […]

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10-Deacetylbaccatins (10 DAB) NATURAL ORGANIC COMPOUNDS USED AS STARTING MATERIAL FOR ANTICANCER DRUGS PRODUCTION

10/10/2018

10-Deacetylbaccatins (10 DAB) are a series of closely related natural organic compounds isolated from the yew tree (Genera Taxus). 10-DAB is also isolated from the needles (leaves) and roots of the Canadian Yew tree, Taxus canadensis, the American ornamental Yew Tree, Taxus media “hicksii” or the European Yew Tree, Taxus baccata, utilizing patented Super Fluid […]

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Difference between C8 and C18 Columns Used in HPLC System

10/05/2018

Difference between C8 and C18 Columns Used in HPLC System About Author Mr. Riaz Akhtar (Zydus Cadila)   C8 and C18 both types of columns are used in pharmaceutical analysis but their use are specific for analysis of different products. Here we are discussing difference between C18 and C8.       High Performance Liquid Chromatography […]

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