Clinical Trial Supply & Procurement

Supporting the advancement of medical science, Silicon Pharma provides specialised clinical trial supply and procurement services. We understand the critical importance of timely and compliant access to investigational medicinal products (IMPs), comparator drugs, and other trial-related supplies to ensure the success and integrity of your research.

Clinical Trial Supply & Procurement

What We Offer - Key Feature

Comparator Drug Supply

Expertise in procuring specific comparator drugs from various locations/countries.

IMP Sourcing

Reliable procurement of Investigational Medicinal Products.

Single Batch & Specific Pack Size Supply

Flexibility to meet precise trial requirements.

No Minimum Order Quantity

Accommodating trials of all sizes, from pilot studies to large-scale phases.

Ongoing Requirements Management

Ensuring consistent and uninterrupted supply throughout the trial duration.

Pedigree Maintenance

Working with reliable partners to maintain product integrity and traceability.

Global Sourcing Capabilities

Leveraging our international network for global trial needs.

Regulatory Compliance

Adherence to Good Clinical Practice (GCP) and Good Distribution Practice (GDP) guidelines.

Our core strengths

Why Choose Silicon Pharma for Global Sourcing?

Reliability

We are a trusted partner in ensuring your trial medications arrive on time and in perfect condition.

Quality & assurance

Commitment to maintaining the highest standards of quality and traceability.

Experienced team

Our specialists understand the intricacies and urgency of clinical trial logistics.

Flexibility

Adapting to the unique and often dynamic needs of clinical research.

Our Process

From initial inquiry and detailed requirement analysis to sourcing, secure logistics, and ongoing supply management, we provide end-to-end support for your clinical trial needs.

Who Benefits

Pharmaceutical companies, Contract Research Organisations (CROs), academic research institutions, and biotech firms conducting clinical trials.