Thursday, June 25, 2020


The manufacturing site conceptualization and designing include the designing of the facility that meets the local and international cGMP requirements as expected by various regulators worldwide. The requirements include and not limited to the layout designing of manufacturing unit, achieving the regulatory expectations of the clean room, Adequate and compliant validation of the Equipment, instruments and utilities and related documentation.

Manufacturing Site Conceptualization Project Services Include Following Stages:

As medical device consultant we do the Manufacturing Plant Design Consulting Services For Medical devices like Orthopedic implants, surgical instrument, dental instrument manufacturing Industry, implant-manufacturing, implantable-moulding, diagnostic-instrument, Active medical devices like EGC machines etc, Disposable products e.g Syringes, IV cannula, IV set, DJ stents etc, Drug-device combination products like Prefilled syringes, Tropical products with applicator, Inhalers etc.

The Manufacturing facility plays the major role in the licencing, certification, regulatory approvals and operating feasibility. Sometimes the compromised design of the facility may bring in irreversible damages on the regulatory approvals and the operational feasibility. During facility design, it is very important to know the current product to be manufactured and possible expected future product regime and their process flow.

Contact details –
Phone no -  9325283428

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