• Central ERP
• Central CRM
• Central Laboratory Information Management System for Laboratories
• Central Warehouse Management System (WMS) for warehouses and investigational medicinal products depots

ALAMERA’s members comply and have received a full implementation program of:
• 21 CFR & ISO certification
• General Data protection regulations (GDPR)
• ISO 9001:2015
• GCLP (Good Clinical Laboratory Practices) for labs
• cGMP and GDP for depots

Each ALAMERA Member has its connections with preferred KOLs, sites, Labs and warehouses in his region and by combining these connections ALAMERA will have a Global Data Network.

As a CRU, this membership will offer a comprehensive package of solutions to support investigators in the development of clinical studies starting from research hypothesis/premises till its full delivery and management support, ensuring the highest International standards of quality and compliance to GCP /ICH guidelines, CFR, EMEA) and National Regulatory Authorities laws.

As an investigator, you will be a member of a research network where you can interact with fellow researchers, share knowledge and practices, ask questions and discuss common topics in clinical research per country, region and therapeutic areas of interest. Find Clinical Trials Opportunities in your region and therapeutic area of expertise. Get access to the latest news and Publications of the therapeutic area of interest. Gain an advantage to develop and acquire certifications in a plethora of modules or trainings in clinical research. Access to a broad list of consultation services to support research from development to publication.
Also, it will covers a comprehensive list which includes any or all of the following:

a. Medical writing (protocols, informed consent, Clinical Study Report, CRF,…etc.)
b. Collaboration with KOLs
c. Submission of study to Institutional review board
d. Data management and Biostatistics
e. Publication (manuscript writing, support, submission to Journals of choice)