Clinical Trial Medication

Ace Pharmaceuticals can assist you in every phase of your clinical research project. From production to distribution of the clinical trial medication.

Ace has extensive experience in sourcing and importing active ingredients, developing and producing all sorts of dosage forms, providing the necessary documentation about the medication for a METC application (IMPD), designing patient packs, taking care of randomisation and organising the distribution to research institutions all over the world. Ace can also perform the necessary analyses.

Production Ace is fully licensed and experienced in producing the most common solid dosage forms (tablet, capsule, granulate) and semi-solid and liquid dosage forms (oral solution, suspension, suppository, creams and ointments). Additionally, Ace can provide sterile and aseptic preparations (infusion bag, vials, ampoules).

Distribution Clinical trial medication can be shipped to research locations worldwide (hospitals, researchers and/or sponsors). Ace takes care of the distribution efficiently and carefully, in collaboration with selected couriers and under highly controlled conditions.

Within the Netherlands, Ace Apotheek (pharmacy) can send clinical trial medication directly to the patients involved.

Quality Assurance Quality is a top priority at Ace. Ace has a manufacturer's license (109098F) and a valid GMP Certificate. Additionally, Ace has a wholesale license, controlled drugs license and license to import active ingredients.

How can we support you in your clinical research? We have a checklist available to prepare a suitable offer, fitting to your needs. Please contact our CTM team to discuss the possibilities. You can reach them by phone at +31 36 547 4098 during work hours or fill in our contact form.