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Pharmaceutical Industry
Pharmaceutical
Industry
Pharmaceutical Industry
Background IntroductionBackground Introduction
  • Collaborative Team
    Includes quality experts, process and equipment experts, design team leaders, construction management experts, validation experts, and operations experts.
  • One-stop
    Includes technology transfer, conceptual design, basic design, detailed design, procurement support, project management, construction management, commissioning and qualification (EPCmV), turnkey contracting (EPC), and facility operations.
Senwo Engineering provides a "one-stop" service for the design and execution of pharmaceutical production facilities, including oral solid dosage forms, biopharmaceuticals, APIs, and sterile product projects, with a "collaborative team" with extensive knowledge and experience.
While facilitating pharmaceutical process transfer (from one institution to another), process scale-up (transitioning from clinical laboratory production to commercial production), and process revision (optimizing capacity across different facilities or changing CDMOs), it ensures product consistency, quality, and compliance.
Available ContentAvailable Content
Technology Transfer
Technology Transfer
T
Technology Transfer
Engineering Design
Engineering Design
E
Feasibility Study
Site Selection
General Layout Design
Planning Design
Conceptual Design
Basic Design
Joint Design (Domestic and Overseas)
Detailed Design and Management
Equipment Procurement
Equipment Procurement
P
Overseas Procurement
Offshore/Onshore Procurement
Subcontractor Management
Construction and Commissioning Confirmation
Construction and Commissioning Confirmation
C
Commissioning Confirmation
Operation and Testing Support
GMP Certification and Product Registration
Facility Operations
Facility Operations
O
Facility Operations
Technology transferTechnology transfer
Methods and stepsMethods and steps
  • STAGE 1STAGE 1
    Planning Feasibility URS STAGE 1
  • STAGE 2STAGE 2
    Process Development Design DQ STAGE 2
  • STAGE 3STAGE 3
    Scale-up Construction IQ STAGE 3
  • STAGE 4STAGE 4
    Training Commissioning OQ STAGE 4
  • STAGE 5STAGE 5
    Production Operation PQ & PV STAGE 5
Our Team
Our Team
With its deep integration of pharmaceutical processes and engineering specifications, Senwo continues to provide global customers with full life cycle services from process transfer, factory construction to operational optimization.
Tyler<br>Thompson
Tyler
Thompson
As a seasoned engineering professional and highly skilled leader, I have extensive experience in delivering major new facility projects within the global life sciences industry. I lead and develop high-performing teams to successfully execute highly complex and challenging programs. I adopt a holistic approach to envisioning optimal directions and establish them clearly through strong communication and negotiation.
Jake <br>McDonald
Jake
McDonald
Pharmaceutical industry expert with over 30 years of experience, specializing in aseptic production, solid dosage form manufacturing, and isolator technology. He previously managed tablet and injectable production facilities in the UK for a renowned pharmaceutical company, served as an international pharmaceutical consultant, and established a "state-of-the-art" injectable filling line facility in Malaysia.
Lachlan <br>Finta
Lachlan
Finta
With over thirty years of experience as an architect, I have been responsible for all phases of design, including master planning, planning, conceptual design, floor plans, design development, construction documents, and management. My career has been dedicated to the technology sector, providing projects for pharmaceutical, biotechnology, and consumer product clients in North America, Europe, and Asia. I specialize in delivering laboratory, office, R&D, and process facilities for life science clients, ensuring compliance with cGLP, cGMP requirements, and adhering to standards and regulations set by NIH, FDA, PIC/S, WHO, and the European Union.
Mika <br>Ye
Mika
Ye
With over 25 years of experience in the pharmaceutical industry, his core expertise lies in regulatory and quality compliance. He has worked with numerous pharmaceutical, medical device, and cosmetic manufacturing facilities to ensure their compliance with EU PIC/S GMP standards and obtain certification.