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How is digital technology helping Indian pharmacists

Express Pharma

The value of India’s retail pharmaceutical market is estimated to touch $59 billion by the fiscal year 2023, which presents a promising opportunity for retail pharmacies to bolster and strengthen their operations. These systems have helped pharmacists efficiently manage their operations, enabling them to generate more revenue.

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Advancement through adversity: how Covid-driven innovations are becoming best practices for pharmacovigilance

Pharmaceutical Technology

AEs can be caused by using medicinal products within or outside the terms of their marketing authorisations (such as off-label therapeutic use, overdose, misuse, abuse or medication errors), as well as from occupational exposure. The following is adapted from a presentation given by Dave Par é and Silvio Scozzari at the DIA 2022 conference.

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What are the elements of quality control process in pharmaceuticals

GMPSOP

– Record or capture all generated raw data directly, promptly, and legibly. – Use traceable data sheets or sequentially numbered notebooks. – Date and sign or initial data entries on the day of entry. – Archive records so that they are protected, secured, and easily retrievable.

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How to perform operational qualification – step by step

GMPSOP

We will present the rationale behind the qualification decision and reference that with the GAMP (Good Automated Manufacturing Practice) categories in support of the decision you will make. The data entry and retrieval process, user access and security, electronic signature, audit trail, system integration, performance, printing, etc.

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Typical GMP documentation in a quality control laboratory

GMPSOP

There are also forms, logs, and registers to keep track of all the little details, as well as product specifications, analytical methods, manufacturing formulae, calculation of raw data and more. Sometime these are labelled as the “hidden factory”. – Ensure systems for archiving of electronic data or notebooks are present.