FAQ

Evimple simplifies the process by allowing you to search through a wide network of verified CDMOs, CMOs, CROs, laboratories and licensing assets, filtered by technology, region, and specific capabilities. It’s designed to help business development managers efficiently find the right partners.

Yes, our platform includes filters for specific technologies such as small molecule development, biologics, drug delivery technologies, and more. You can narrow down your search based on your project needs.

Once you find a suitable partner, you can access the contact information of the responsible person within the company. This information is available in the company's profile, which you can unlock using credits from your subscription. This allows for direct and smooth communication between you and the supplier.

Yes, Evimple operates on a subscription basis. Clients need to purchase an annual subscription, which includes a basic number of credits. These credits can be used to access the contact information of potential partners. For users with more extensive needs, additional credit packages can be purchased throughout the duration of the subscription.

Yes, you can send a request for proposal (RFP) through the platform. Suppliers and service providers will respond with detailed bids based on your project requirements.

Evimple is a platform that connects CDMOs, CMOs, CROs, laboratories and drugs developers with pharmaceutical companies looking for partners. It streamlines the process of finding clients, managing inquiries, and fostering collaborations through a business development-focused platform.

To register, contact us, fill in the required information in the questionnaire, and submit your profile. Our team will review your submission and verify your details before listing your company on the platform.

No, listing your services on Evimple is free. You can create a profile and showcase your offerings at no cost.

Yes, you can log in at any time to update your profile, add new services, or change your company’s information.

We conduct a thorough verification process, including reviewing certifications (e.g., USFDA, EU GMP) and references to ensure credibility and quality.