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Pharmaceutical Turnkey Project Solutions

HMPL - Given the significance of the pharmaceutical industry in the society, we make it a point to bring together some of the Latest advances in manufacturing practices and technology.

Pharmaceutical Turnkey Project Solutions

HMPL - Given the significance of the pharmaceutical industry in the society, we make it a point to bring together some of the Latest advances in manufacturing practices and technology. All our services and offerings, along with the technology being used, comply with the national and international standards and norms, as established by some of the renowned regulatory authorities including FDA, UNHCO, WHO and cGMP among others.

With our vast network of experts and mix of global and local supplier, HMPL is a perfect place to undertake complex and unique projects and deliver quality and timely solutions meeting regulatory requirements.

HMPL can work in different combinations of responsibilities depending on customer requirements.

It can be an EPC (Engineering, procurement and construction) contract including complete construction of infrastructure and supply and commissioning of production machinery and systems or

it can be a procurement management contract whereby HMPL supports only in procurement and qualification of machinery and supports system whereas construction of infrastructure is taken care by customer locally.

HMPL with its team of experts who have extensive knowledge, can suggest the best equipment, machinery and system with the right cost and quality.

HMPL – STANDARD STEPS: HMPL – PROPOSES RELIABLE KNOW HOW & TECHNOLOGIES ABOUT: HMPL – PERFORMS A TURNKEY PROJECT THROUGH:
Basic Engineering LVP (Large Volume Parenterals) & SVP (Small Volume Parenterals) in PVC or PP bags Procurement of Licensors and Know How Transfers
Detailed Engineering LVP in Glass or Plastic Bottles Conceptual Design and Design Qualification (DQ)
Design Qualification SVP (Small Volume Parenterals) in Glass or Plastic Vials and Ampoules Detailed Engineering
Inlet Water Pretreatment Plant Pre-filled Syringes Validation Master Plan & S.O.P.
Pharmaceutical Water Systems (Softened, Purified and Distilled Water) Oral liquids & Solid dosage Equipment Construction & Procurement
Pharmaceutical Processing and Solution Preparation Systems Multipurpose Pharmaceutical Plants Factory Acceptance Test (FAT)
Pharmaceutical Forming, Filling, Inspecting, Packaging lines Dialysis concentrate solutions and powders (Canisters, Bags, Cartridges) Shipment and Installation
Clean Rooms Plasma Fractionation Site Acceptance Test (SAT)
Epoxy coating of the floors Biotechnological Plants Standard & Validation Documentation (IQ/OQ/PQ Protocols)
HVAC and air treatment plant Training
Pure Steam Generator and PS circuitAutoclave Commissioning, Calibration & Start up
Laboratories of Analysis (Microbiological / Chemical) Regulatory Support
Site Master Plan
Validation Master Plan
Installation
Training
Start up
Technical Files
Documentation
IQ/OQ
PQ Protocols
Validation at Site
Standard Operating Procedures
Initial Know How Transfer
GMP pre Audit
Spare parts for n years

Headquarter

Reach out to Syntegon.
india
Vatva Ahmedabad, Gujrat

Phone

+1(365) 567 89 54
+800 350 84 31

Social

Email

info@harikrushna007.com

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