We are experienced in the validation and Stability Chamber Maintenance Services. We stand outs from others by our approach to services and technically superiority. We take our every validation project as a challenge to meet our clients need by considering all regulatory guidelines.
It has often been seen that validation professionals from pharmaceutical companies are lack of practical experience in relation to the development and use of Programmable Logic Controller (PLC) application software. Understanding and configuring today’s software packages are easier than ever before; however validation of automation systems is indeed an exertion task. We perform the HVAC validations as per ISO 14644- 1, 2, 3, EU GMP/EC GMP, WHO-TRS-937, WHO-TRS-961, Schedule M (National Regulatory Body) guidelines for all room classifications. Methods for evaluation and measurements for Certification are specified in ISO14644-3.
Our emphasis is on current good engineering practice (GEP) which ensures that engineering methodology generates deliverables that support the requirement for qualification or validation as per the pharmaceutical industry requirement.
Our procedures are in accordance with National/ International regulatory authorities like USFDA, MHRA, MCC, TGA, WHO (Geneva) and ISO.
Passion, Commitment, Dedication, Ability, Initiative, Reliability, Loyalty, these attributes characterize and distinguish us and allow us to tackle the challenges that we are called upon to deal with every day.
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