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Trusted Standards. Global Confidence.

At Dew Lifecare Inc., quality is more than a regulatory requirement — it is the foundation of every product we deliver. As an export-focused pharmaceutical company, we understand the responsibility that comes with serving diverse international markets, and we take pride in upholding global quality benchmarks at every stage of our operations.

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Our Commitment to Quality

We implement a comprehensive quality assurance framework designed to meet the stringent expectations of international health authorities. Every product undergoes rigorous testing, documentation, and validation before it reaches our clients — ensuring not just compliance, but confidence.

Certifications & Regulatory Approvals

Dew Lifecare Inc. works exclusively with audited manufacturing partners who are certified by leading global regulatory agencies. Our supply chain is built on a foundation of credibility and traceability.

We support and maintain:

  • WHO-GMP certified manufacturing facilities
  • ISO 9001:2015 and ISO 13485:2016 (for medical devices and diagnostics)
  • CE Certification for IVD products and surgical consumables
  • MOH approvals in key international markets (including Kenya, Nigeria, Ghana, Tanzania, and more)

Each certification reflects our unwavering focus on product safety, process integrity, and documentation discipline.

Ongoing Compliance

We actively monitor regulatory updates in each country we export to, and assist our clients with:

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    Dossier preparation and product registration

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    Technical documentation and COA management

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    Batch certification and stability data support

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    Post-market pharmacovigilance and audit readiness

Reliability in Records

Testing & Documentation

All products meet international pharmacopeial standards (IP/BP/USP/Ph. Eur.). Stringent in-process and finished product testing is conducted under validated protocols — backed by robust documentation trails and digital batch records where applicable.