Announcement

UPDATE AS OF 15.05.2024!!!

We are pleased to announce that the competition proceedings have ended, accepting one application, which was submitted by Biostat Ltd. We thank all potential participants for their interest. According to the result, the selected referee is Biostat Sp. z o. o. company. Detailed information on the next steps will be provided to the successful consortium member.

The offer is aimed at entities:

1. Having the status of a Research and Development Center or other equivalent, allowing the conclusion of a consortium under the conditions indicated in the competition regulations ABM/2024/1. The criterion will be considered fulfilled after the Bidder presents a statement along with documents confirming the implementation of the system (if available).
2. Having experience in organizing and monitoring clinical trials, observational studies or medical research experiments funded by the Medical Research Agency (at least 10 ongoing projects or 5 completed). The criterion will be considered fulfilled after the Bidder provides a statement with a list of projects.
3. Having experience in the organization and monitoring of clinical trials, observational studies or medical research experiments funded by the Medical Research Agency understood as completed and settled projects of at least PLN 1,500,000 net. The criterion will be considered fulfilled after the Bidder provides a statement with a list of projects.
4. Having at their disposal a team member or team members with at least five years of documented experience in managing observational studies or research medical experiments. This criterion will be considered fulfilled upon submission of a statement by the Bidder along with a resume of the proposed team members.
5. Having at their disposal a team member in the position of medical writer or equivalent, with at least five years of experience in developing protocols for clinical trials, observational studies or research medical experiments(including at least 3 research medical experiment protocols). The criterion will be considered fulfilled upon submission of a statement by the Bidder along with a resume of the proposed team members.
6. Having an electronic Clinical Observation Card (eCRF) system used in at least 20 clinical trial, observational study or medical research experiment projects. The criterion will be considered fulfilled after the Bidder provides a statement with a list of projects.
7. Having its own system of Standard Operating Procedures(SOP) for conducting clinical trials, observational studies or research medical experiments. The criterion will be considered fulfilled after the Bidder submits a list of operating procedures.

Does the contracting authority allow subcontracting: No

Rules of the contest available here.

Please send your applications to email: marketing@paleyeurope.com