The hemarsh's Podcast

The Benefits of Custom Synthesis and Reference Standards

Hemarsh Technologies was established in 2008 and since then our company has enjoyed a rapid growth. Our prime focus is on contract research and impurities synthesis for pharmaceutical industries. We provide well characterized reference standards essential to ensure accuracy and validity of analytical methods used with-in the pharmaceutical industry. For more information, please visit our website www.hemarsh.com

What is Reference Standard in Pharma Industry?

Hemarsh Technologies was established in 2008 and since then our company has enjoyed a rapid growth. Our prime focus is on contract research and impurities synthesis for pharmaceutical industries. We provide well characterized reference standards essential to ensure accuracy and validity of analytical methods used with-in the pharmaceutical industry. For more information, please visit our website www.hemarsh.com

What is Impurities Synthesis?

Hemarsh Technologies was established in 2008 and since then our company has enjoyed a rapid growth. Our prime focus is on contract research and impurities synthesis for pharmaceutical industries. We are also leading impurities suppliers in India. For more information, please visit our website www.hemarsh.com

Pharmaceutical Impurity Standards

Impurities Standard Suppliers and their Importance

'Impurities' refers to synthetic impurity standards and known metabolites of APIs that have been resynthesized to the highest purity, and are supplied with full analytical data, allowing precise identification and quantification of extraneous molecules that may be present in a drug.
 
 

IMPURITIES AN OVERVIEW | API impurities | Hemarsh Technologies

Impurities in pharmaceuticals are the unwanted chemicals that remain with the active pharmaceutical ingredients (APIs), or develop during formulation, or upon aging of both API and formulated APIs to medicines.
 
 

IMPURITIES AN OVERVIEW | API impurities | Hemarsh Technologies

Impurities in pharmaceuticals are the unwanted chemicals that remain with the active pharmaceutical ingredients (APIs), or develop during formulation, or upon aging of both API and formulated APIs to medicines.
 
 

Different Types of Impurities in Pharmaceuticals

The impurities in pharmaceuticals are organic or inorganic material, or residual solvents other than the drug substances or ingredients that arise out of synthesis or unwanted chemicals that remain with the active pharmaceutical ingredients (APIs) or develop during formulation or upon aging of both API and formulation.

Indian Pharma – Key Trends And Predictions | Indian Pharmaceutical Industry

Hemarsh Technologies –Doxycycline impurity C manufacturer and suppliers in India. We are leading manufacturer and supplier of Drug Impurity standards.
 

Identifying Impurities in APIs

Hemarsh Technologies – Active Pharmaceutical Ingredient (API)  impurities suppliers. We are a leading manufacturer and supplier of API impurities.