Turnkey Cleanroom Solutions

GMP modular walls have been installed in clean rooms throughout the world in a range of applications from API manufacturing to Sterile manufacturing units. The system is readily adaptable to meet requirements of most clean room classifications as determined by cGMP grades used in pharmaceutical applications.

Our Fire rated doors are approved by Warringtonfire UK & Underwriters Laboratories. The accessories used for these doors are from reputed brands, to make these doors of international standards.

Cleanroom equipments are of utmost importance for their intended use. All these equipments come with factory tested certificates and documentations. All GMP products are manufactured under one roof and subsequently all metal finishes, assembly are completed in-house. As a result, specific requirements of client can be incorporated into a proposed design.

Customised HVAC systems & solutions are designed & engineered by experts having immense experience in designing the Pharma & Biotech Plants. Our HVAC design is strictly based on the different guidelines and regulations set by authorities.

We provide energy efficient electrical systems that provide maximum level of safety and require minimum maintenance. We design customized electrical systems considering specific project requirements along with compliance to relevant International codes. We take into account fundamental principles of energy conservation and safety that encompass protection against electric shocks, thermal effects, over current, fault current and over voltage.

GMP Technical Solutions develops bonding, sealing, damping and reinforcing solutions for the Pharmaceutical & related industries, for manufacturing, Packing & Stores.

BMS with open architecture and Lonworks / Bacnet compatible DDCs Pharma Suite : 21 CFR Part 11 compliant validation software.As an engineering solutions provider, GMP takes responsibility for design, supply, installation, commissioning and maintenance, offering end-to-end solutions, energy management and comfort throughout the life-cycle of the system.

Piping is critical in terms of design and is of utmost importance for any successful Pharmaceutical or Biotech facility. As it employs very high initial set-up cost and routine maintenance, its design has to be ideal and cost effective.

In accordance with the recommendations from International Standards, GMP establishes a Commissioning and Qualification plan based on Risk analysis that permits the classification of the various systems and its components depending on their impact on final product quality. We supervise projects all around the world. Together with our partners, we guarantee top-quality installation and supervisory operations. Specially trained professionals are provided to perform demanding commissioning tasks and particle and classification measurements within the field of clean room technology.