FAQ’s

At Synergy, we follow a structured and transparent registration process:

1. Initial Consultation – Understanding your product and target markets (GCC or Africa).

2. Documentation Review – We assess the available technical documents and identify any gaps.

3. Dossier Preparation – Compilation of regulatory documents as per country-specific requirements.

4. Submission to Authorities – We coordinate with health ministries or regulatory agencies in your chosen region.

5. Follow-Up & Approval – Regular follow-ups until the final registration certificate is issued.

We provide registration consultancy for the following categories:

• Pharmaceuticals (finished formulations, APIs, etc.)

• Nutraceuticals (dietary supplements, vitamins, health products)

• Surgical Products (medical devices, instruments, disposables)

If your product falls under any of these categories and is manufactured in compliance with Pakistani or international GMP standards, it is generally eligible for registration.

The timeline depends on the product category and target country, but typically:

• Pharmaceutical Products: 6 to 12 months

• Nutraceuticals: 4 to 8 months

• Surgical Products: 3 to 6 months

We always provide realistic timelines after evaluating your product and documentation.

The exact requirements vary by country, but commonly requested documents include:

• Company Profile

• Product Composition / Formula

• Manufacturing License

• Free Sale Certificate

• GMP Certificate

• Certificate of Analysis (COA)

• Stability Data (for pharmaceuticals)

• Packaging & Label Designs

• Product Samples (when needed)

Our team will provide you with a detailed checklist tailored to the product and target region.