Diagnostics
We partner with investors, startups, VCs, and banks to deliver end‑to‑end pharmaceutical and healthcare ventures — from greenfield facility plans to product development, regulatory approvals, and launch.
Our turn‑key model covers RFP and vendor/CDMO selection, site visits and negotiations, technology transfer, quality systems, clinical and regulatory strategy, and market access — providing a single accountable partner.
What We Deliver for Investors
Comprehensive turn‑key execution across facilities, products, and compliance — aligned with regional and global requirements.
- Pharmaceutical facility development (API, finished product, excipients) — GMP‑compliant design.
- Product development across pharmaceuticals, nutraceuticals, and cosmeceuticals.
- Regulatory affairs across DRAP, FDA, EMA, MHRA, GHC , MENA and SFDA.
- Market research, competitive analysis, licensing, and partnerships.
- Clinical trials coordination and compliance support.
- RFP management, vendor/CDMO shortlisting, site visits, and negotiations.
- Technology Transfer: Methods, Materials, Processes, and Documentation.
RFP & Vendor Selection
Define scope, issue RFPs, compare proposals, and shortlist CDMOs/CROs using cost, quality, and compliance criteria.
Site Visits & Negotiation
Coordinate 2–3 site visits, evaluate capabilities, negotiate contracts, and select primary and backup partners.
Technology Transfer & Launch
Transfer methods, materials, and processes; stand up QMS; and prepare regulatory and market access packages.
Our Approach
A single accountable partner from feasibility to launch — integrating technical, regulatory, financial, and operational workstreams.
- Transparent governance: milestones, KPIs, and risk registers.
- Vendor oversight with audits, change control, and quality gates.
Execution & Compliance
Stand up operations with Qualified Partners, Technology Transfer packs, and Regulatory submissions per market.
Vendor/CDMO
Clear guidance, negogiation support and qualification.
Investor Partnerships & Delivery Network
We leverage a network of CDMOs, CROs, clinical sites, and healthcare builders to deliver compliant, cost‑effective projects.
Facility Development
cGMP‑compliant API, finished product, and excipient plants with validation plans.
Product & Regulatory
Development plans, licensing/partnerships, and filings across DRAP, FDA, EMA, MHRA, GHC, MENA and SFDA.
Healthcare Build‑Out
Hospitals, Clinics, Diagnostics, Pharmacy Chains, Accreditation (ISO/JCI/NABH), and QMS.
Frequently asked questions about Turn‑Key Consultancy
Facility development, product development, regulatory affairs, market research, licensing/partnerships, clinical coordination, and compliance.
We run structured RFPs, shortlist vendors, conduct site visits, negotiate, and manage delivery with KPIs and quality gates.
Yes — we coordinate filings and responses across DRAP, FDA, EMA, MHRA, SFDA, MENA and GHC regulators.
We plan and deliver Hospitals, Clinics, Diagnostic Labs, and Pharmacy Chains, including ISO/JCI/NABH Accreditation programs.
Yes — we provide asset evaluation, risk/gap analysis, capital estimates, and tracking for investor/bank decision‑making.