Offers services for the design, implantation and revamping of installations, from concept to commissioning on the turnkey concept. Moreover, is also a supplier of cleanroom products, instruments and equipment.
Our company offers Turnkey Services for setting up of Pharmaceutical and Process Industry projects as per WHO, GMP, USFDA, PICS, MHRA, TGA and EU GMP guidelines. Our expertise is acknowledged by several high profile projects successfully completed in international segments.
PIS ENGINEERING is a Cleanroom Turnkey Solution provider specializing in design, manufacturing, construction, commissioning and validation services of cleanrooms and associated controlled environment.
With over 15 years’ experiences in the field of cleanrooms and associated controlled environment, PIS ENGINEERING has cultivated an in-depth understanding and expertise of executing cleanroom turnkey projects. PIS ENGINEERING’s cleanroom system providers an ultra-clean environment ranging from Class 10(ISO-4) to Class 100000(IS0-8) with effective control of air flow, pressure, temperature, relative humidity and filtration suitable for various cleanroom applications, such as pharmaceuticals, microelectronic, hospital, food, lab, etc.
Integration is the single most important activity for a Pharmaceutical project. Pharmaceutical Projects are complex in nature, having following features
At PIS ENGINEERING, we integrate, articulate & unify the entire sub-processes into a cohesive whole. Project Integration is our USP. With our vast experience in handling International Pharmaceutical Projects, we ensure that professional integration of project will have plenty of benefits to you like…
Last but not the least, Project Integration is not a limited to brick and mortar, it is integration of like-minded companies/individuals for a long term Association.
As a turn-key provider of machinery, automated assembly systems and packaging for the pharmaceutical and medical device industries, we take full responsibility for the designing, building, testing, commissioning, and servicing of standard or fully automated pharmaceutical systems.
At PIS ENGINEERING we service the following industries:
URS
Project & Quality Plan
cGMP Layouts
cGMP Flows
PFDs
Clean Room & AHU Zoning
Automation Philosophy
Budgetary Estimates
Architectural Drawings
Structural Drawings
HAZOP Studies
Equipment Layout
Room Data Sheets
Technical Specifications
Tender Documents
Revised Budgetary Estimates
Project Schedule Tracking
Validation Master Plan
Risk Analysis
Impact Assessment
Qualification (DQ/IQ/OQ)
F.A.T Services
S.A.T Services
Preparation of SOPs
Vendor Evaluation
Tender Evaluation
Procurement Schedule
Cash Flow Management
Stage Wise Management
Stage Wise Inspection
Document Verification
P & IDS
Capacity & Cycle Time Analysis
Equipment Rationalization
Utility design, sizing and layout
Process Automation
Entire Project Management
CADMATIC – 3D Virtual walk through design
EloDoc – Comprehensive Document Management Software
On site Execution & supervision support
Mock Audits
PIS Engineering designs, constructs, commissions and validates legal and technical infrastructures that maximizes technological creativity, and innovation.
PIS Engineering offers Turnkey Services for setting up of Pharmaceutical and Process Industry projects as per WHO, GMP, USFDA, PICS, MHRA, TGA and EU GMP guidelines.
Our highly trained product experts can work directly with your teams and triage your related problems, providing 24/7 maintenance of valuable solutions.
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