Preparing equipment and facilities for regulatory audits
In the highly regulated environment of the pharmaceutical industry, audits and regulatory inspections are a constant. The adequate […]
Annex 11 of the GMP enters public consultation: key changes to adapt to the digital era
Annex 11 of the GMP details the requirements for the use of computer systems in manufacturing and
SCADA SYSTEMS VALIDATION IN CHEMICAL AND PHARMACEUTICAL PLANTS
In the chemical and pharmaceutical industry, SCADA systems (Supervisory Control and Data Acquisition) play a critical role in the
Understand the stages of qualification and its impact on pharmaceutical quality
In the pharmaceutical industry, where the quality, patient safety and compliance with regulations are priority, qualification
Annex 11 GMP and the quality guarantee in computerized systems: a pillar of pharmaceutical regulation
The pharmaceutical industry, due to its intrinsic relationship with public health, is subject to a rigorous regulatory framework that guarantees
Technical Life Cycle of Pharmaceutical Projects: Focus from Engineering
The development of a project in the pharmaceutical industry requires meticulous planning, multidisciplinary coordination and compliance with regulations
Connect, collaborate, advance: communication as a equipment engine
In any organization, effective communication is much more than a simple exchange of information. It is the basis on the
The strategy behind the design of modern API facilities
The design of facilities for the production of active pharmaceutical ingredients (API)
Growing together: 10 questions to our CEO
On the occasion of IDE Pharma & Chemistry Engineering S.L. anniversary, we talked with Francisco Arguimbau, CEO of the company, for
Validation as a guarantee of control in control systems
In the pharmaceutical industry, guaranteeing the quality, safety and effectiveness of products is an absolute priority. To do this, I know