Comprehensive pharmaceutical advisory

The plus of confidence for your industry

Founded by specialists who have worked inside the regulator — AEMPS and EMA — we help the pharmaceutical and life-science industries decide with confidence.

EMA assessor experience Court expert · COFM / UICM UNE-EN ISO/IEC 17025 auditor
Pharmaceutical industryCosmeticsFood supplementsThird-party analysisBiotechnologyPublic administration
25+
Years of industry experience
12
Years at the Spanish Medicines Agency
4
Specialised services
6
Sectors we serve
Why Afiplus

A close partner with proven experience

Our advisors have built their careers in industry and in public agencies (the Spanish Medicines Agency — AEMPS — and the EMA), holding positions such as Qualified Person and Quality Assurance Director.

  • Quality as our cornerstone. Our working philosophy is defined by our own quality policy.
  • Tailor-made solutions. Quality systems adapted to each company and each moment.
  • Real experience. Years of hands-on practice in the manufacture, control, regulation and auditing of medicines.
  • On-site or remote audits. We adapt to the way your company operates.

Meet the team

Trust

Absolute confidentiality and a public code of ethics guiding every engagement.

Proximity

Direct contact with the consultants who do the work — no intermediaries.

Rigour

Methodology aligned with GMP, GDP, ISO 17025 and the ICH guidelines.

Facing a technical, regulatory or quality challenge?

Tell us about your case with no obligation. We will analyse your need and propose a realistic, tailored solution. We reply within 24 working hours.

Contact us now