About ALVEDA
An integrated partner for pharmaceutical projects.
ALVEDA Pharma Project is a pharmaceutical engineering and project consulting practice. We work across the project lifecycle, from feasibility and concept design to commissioning, qualification and handover. Our role is to keep engineering, compliance and delivery decisions aligned.
How we work
Coordinated disciplines
Architecture, HVAC, utilities, process and automation are developed in one coordinated model. Interfaces between disciplines are resolved in design, not on site.
Compliance embedded early
GMP requirements, cleanliness grades and qualification needs are set at concept stage. The URS and the design basis carry them through every later stage.
Decisions documented
Design decisions, assumptions and changes are recorded and traceable to requirements. The same record supports DQ, IQ, OQ and PQ.
Why ALVEDA
How we approach a pharmaceutical project.
- 01
Integrated Thinking
Engineering disciplines coordinated around one pharmaceutical project strategy.
- 02
Compliance by Design
Operational and regulatory considerations embedded early in the design process.
- 03
Execution Focus
Engineering solutions developed with constructability, operation and project delivery in mind.
- 04
Digital Coordination
Modern tools, documentation and coordination supporting more informed project decisions.
Project Lifecycle
One Partner. Across the Project Lifecycle.
Decisions made at feasibility shape what is qualified at the end. We carry one technical basis from the first study through commissioning and qualification.
- 01
Discover
Assess the product portfolio, capacity, site options and a feasible investment envelope.
- 02
Define
Capture user requirements, regulatory basis and design criteria in an approved URS.
- 03
Plan
Set the master plan, phasing, budget, schedule and validation strategy.
- 04
Design
Develop coordinated architecture, cleanroom, HVAC, utilities and process design through DQ.
- 05
Procure
Specify, tender and evaluate equipment packages; witness FAT before shipment.
- 06
Build
Construct and install to approved drawings under documented site quality controls.
- 07
Commission
Start up, test, adjust and balance systems; complete SAT and punch lists.
- 08
Validate
Execute IQ/OQ/PQ protocols and compile evidence that systems perform as intended.
- 09
Operate
Support handover, SOPs, maintenance planning, periodic requalification and change control.
Values
- 01Precision
- 02Compliance
- 03Engineering
- 04Trust
- 05Execution
The aim on every project is the same: a facility that can be operated, maintained and qualified as intended.
Next step
Planning a pharmaceutical project?
Share the product type, the current stage and the main constraints. We will respond with a proposed scope and next steps.
+20 101 171 1700