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Pharmaceutical Consulting · Ghana & Africa

Precision · Compliance · Growth

Navigate Africa's
Pharmaceutical
Landscape with Confidence.

SCS Pharma Consult bridges the gap between science, regulation, and profitability — helping manufacturers, distributors, and investors build structured, compliant, and scalable pharmaceutical systems across Ghana and Africa.

Start Your Engagement → Explore Our Services
4
Core Service Pillars
FDA
Ghana Regulatory Experts
Pan-Africa
Market Coverage
100%
Compliance-Driven
The Challenge

Industry Problems We Eliminate

Ghana's pharmaceutical sector is undergoing rapid transformation. These are the friction points we systematically resolve for our clients.

⚠️
Failed FDA Inspections
⏳
Delayed Regulatory Approvals
📋
Poor SOP Documentation
💸
Cash Flow Mismanagement
🔗
Weak Supply Chain Systems
📊
Compliance Framework Gaps
SCS Pharma Consult

Samuel E.K. Agyei

Managing Director
Who We Are

Ghana's Premier Pharmaceutical Consulting Firm

SCS Pharma Consult is a pharmacist-led consulting firm operating at the intersection of science, regulation, and business strategy. We deliver structured, execution-focused solutions that help pharmaceutical organisations navigate Ghana and Africa's evolving regulatory landscape.

🎯

Our Mission

Build structured, compliant, and scalable pharmaceutical systems across Ghana and Africa — bridging science, regulation, and profitability.

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Our Philosophy

Zero dependency on informal channels. Documentation-driven approvals. Ethical regulatory engagement. Zero tolerance for compliance breaches.

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Our Reach

Serving pharmaceutical manufacturers, importers, distributors, hospitals, research institutions, and investors across Ghana, West Africa, and beyond.

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Our Authority

Pharmacist-led team with deep regulatory depth. We combine technical expertise with a scalable system design to deliver lasting compliance value.

What We Do

Our Four Service Pillars

End-to-end pharmaceutical consulting — from regulatory clearance to enterprise growth strategy.

01
📜

Regulatory & Compliance Advisory

We eliminate preventable FDA delays through structured pre-submission audits, dossier validation, and active query management — targeting 6–9 month approval timelines versus the industry norm of 12–18 months.

  • FDA Ghana product registration (CTD format)
  • GMP & GDP advisory and inspection readiness
  • Dossier preparation, evaluation & gap analysis
  • Post-approval variation management
  • 48–72 hour query response protocol
02
🏗️

Pharmaceutical Business Structuring

From licensing roadmaps to full organisational architecture, we build compliant operational foundations for pharmacies, wholesalers, and pharmaceutical businesses entering the Ghanaian market.

  • Pharmacy & wholesale establishment setup
  • Licensing roadmaps and regulatory milestones
  • SOP development and staff training
  • Organisational architecture & governance
  • Good Pharmacy Practice (GPP) compliance
03
🔄

Supply Chain Optimisation

We design and implement pharmaceutical supply chain systems that reduce cost, improve inventory accuracy, and build vendor resilience — giving you operational control from procurement to dispensing.

  • Procurement strategy and sourcing frameworks
  • Inventory management systems design
  • Vendor evaluation and qualification
  • Distribution and logistics cost optimisation
  • Cold chain and storage compliance
04
📈

Enterprise & Investor Advisory

Positioning pharmaceutical businesses and investment portfolios for sustainable growth across Ghana and Africa. Strategic market entry, expansion planning, and financial structuring for enterprise-scale engagements.

  • Market entry strategy — Ghana, ECOWAS, Pan-Africa
  • Investor due diligence and advisory
  • Portfolio expansion and prioritisation planning
  • Financial and operational structuring
  • Leadership advisory and governance design
Our Process

From Intake to Outcome

A structured, transparent engagement model — you always know where your file stands.

01
Client Intake
Submit your intake form. We review your scope, products, and regulatory goals.
02
Proposal & Agreement
Receive a tailored proposal with clear fees, timelines, and deliverables. Sign your Service Agreement.
03
Dossier Audit
Our team performs a full pre-submission audit, eliminating 60–70% of avoidable deficiencies.
04
Submission & Tracking
Structured submission with active query monitoring, dedicated follow-up, and regular status reports.
05
Approval & Beyond
Registration secured. We continue with lifecycle management, variations, and portfolio expansion.
Transparent Pricing

Clear Fees. No Surprises.

✓ All fees in USD · GHS accepted at Bank of Ghana rate

Our pricing is transparent, structured, and tied to deliverables — not billable hours.

Regulatory Services — Standard Fees
Service Fee (USD) Payment Terms Notes
Supplement Registration
Dossier Preparation & FDA Ghana Submission
 $600
per SKU
 50% upfront · 50% on registration number issued Per SKU
Supplement Dossier Evaluation
Technical Review of existing dossier
 $100 100% due on document receipt —
General Drug Registration
Full dossier preparation & FDA Ghana submission
 $1,500
per SKU
 50% upfront · 50% on registration number issued Each additional SKU: $300
Drug Dossier Evaluation
Technical review of existing dossier
 $300 100% due on document receipt —
Business Structuring / Supply Chain / Investor Advisory
Bespoke engagements
 Custom As per formal Pro Forma Invoice Bespoke engagement
Retainer & Package Consulting
Starter
Compliance Foundation
$1,000
– $2,000 one-time setup
+ $800 / month retainer
  • Compliance audit & gap analysis
  • SOP development (core set)
  • GMP/GPP advisory sessions
  • Monthly compliance report
  • Email & call support
Best for: Small pharmacies & new entrants
Regulatory
Registration Track
$2,500
– $6,000 per engagement
+ $1,500 / month retainer
  • Full dossier preparation & submission
  • Pre-submission audit included
  • Unlimited query management
  • Artwork & label compliance review
  • Regulatory dashboard reporting
Best for: Product registration clients
Most Popular
Full Setup
Pharmacy & Wholesale
$6,000
– $10,000 full setup
+ $3,000+ / month retainer
  • End-to-end pharmacy/wholesale setup
  • Full licensing roadmap
  • SOP suite & staff training
  • Supply chain system design
  • Ongoing compliance retainer
  • Quarterly audit readiness check
Best for: Medium wholesalers & growing operations
Enterprise
Strategic Advisory
$18,000+
custom engagement
Retainer by agreement
  • Full enterprise advisory mandate
  • Market entry & expansion strategy
  • Investor due diligence support
  • Portfolio management & reporting
  • Board-level regulatory intelligence
  • Dedicated relationship manager
Best for: Manufacturers, PE firms & large distributors

Important: Government statutory fees, FDA Ghana filing fees, and third-party charges are not included in SCS Pharma Consult consulting fees and are borne separately by the client.  |  Payments accepted in USD or GHS (at Bank of Ghana rate on payment date) via bank transfer to Guaranty Trust Bank, Ghana.

Start Your Engagement

Client Intake & Onboarding Form

Complete this form to initiate your formal engagement with SCS Pharma Consult. We'll review your submission and respond within 48 hours.

SCS Logo

SCS Pharma Consult

Client Intake & Onboarding Form · SCS/CIF/2026

v1.0 · April 2026
Section A — Client & Company Details
Section B — Service Requirements
Section C — Budget & Fee Acknowledgement

Standard Fee Schedule (for reference)

  • Supplement Registration (Dossier Prep & Submission): USD $600.00 per SKU
  • Supplement Dossier Evaluation (Technical Review): USD $100.00 — 100% due on document receipt
  • General Drug Registration (Dossier Prep & Submission): USD $1,500.00 per SKU; each additional SKU: $300
  • Drug Dossier Evaluation (Technical Review): USD $300.00 — 100% due on document receipt
  • All other services: Fee as per formal Proposal / Pro Forma Invoice
Section D — Confidentiality
All information submitted is received in strict confidence. SCS Pharma Consult will not disclose, share, or distribute any proprietary or commercially sensitive information to any third party without prior written consent, except as required by Ghanaian law. This confidentiality obligation survives termination of any engagement.
Section E — Documents Available
Declaration & Submission

Your submission is encrypted and handled in strict confidence.

Get In Touch

Let's Talk About Your Regulatory Goals

Whether you're registering a first product, scaling a portfolio, or entering the Ghanaian market — we're ready to engage.

✉️

Email

scspharmaconsult@outlook.com
📱

WhatsApp

+233 20 902 6800
📍

Location

Ghana, West Africa

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Markets Served

Ghana · West Africa (ECOWAS) · Pan-Africa · International

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We'll respond within 24–48 business hours.

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