Important information regarding the contacts and business relationships that you make through the B2B MARKET PLACE, keep in mind that:

PROCOLOMBIA accompanies companies with the purpose of facilitating business opportunities between exporters and buyers, without intervening in purchase and/or sale decisions, therefore, the contractual and legal responsibility of commercial negotiations falls directly on the companies that carried out the commercial transaction (exporter and buyer).
Although PROCOLOMBIA carries out a preliminary investigation of the companies as part of its work methodology and commercial management, this process does not constitute any guarantee of compliance in the negotiations between the parties, for this reason it is recommended that both the exporter and the buyer carry out their own validations and protect their commercial operations with the mechanisms available in international trade regulations.
The relationship between PROCOLOMBIA and the companies in Colombia and abroad, is generated through trust and the experience acquired from previous actions; however, such companies may present situations that could lead to possible breaches, without these being the responsibility of PROCOLOMBIA, which is why both exporters and buyers must ensure that they use secure negotiation tools, seek advice from experts to assess commercial risks and formalize the contractual documents that may be necessary to shield their conversations.
ProColombia will in no case be responsible for the information of the companies and/or products available on this platform since it is filled out completely by each one of the companies.

PFS II (Patient Follow-up System)

PFS is a web system intuitive and easy-to-use tool for monitoring the clinical trial participants and the whole trial. Therefore it is the application where all the information collected by our TrialPal is centralized. A specialized software based on highly reliable and available platforms that guarantees an excellent service performance without interruptions, integrating security standards, and guidelines such as CRF Part 11 from the FDA. This system is designed mainly for the Sites and will allow efficient management of subjects and the trial.

Category :
Software & IT services
Subcategory:
Health Software

Company

INTEGRA IT SAS

We are the first technology company in the Life Science industry to serve clinical trials and patient programs in Latin America integrating data from patients, sites, CROs, and Sponsors. With global reach and US-based, we have created agile, flexible, and validated-secure solutions that use real-time data from patients to sponsors to improve decision-making, reduce costs and contribute to the world's health and quality of life.
We offer a solutions suite 100% cloud-based, in compliance with the 21 CFR Part 11 guidelines from the FDA and the GCP (Good Clinical Practices). Our purpose is to make clinical trials' performance more efficient through high-end technology while making them person-centered. https://integrait.co/home1

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