Bioforum was founded in 1998 as a center for applied knowledge, providing training and education activities to the biomedical, pharmaceutical and medical device industries. As the company grew, the Bioforum team expanded the service to include outsourcing solutions in the clinical area and expert consultation. Our activities serve and upgrade the performance of our clients and their products. We maximize our costumers’ benefits by providing cost effective outsourcing and consultation services. About 10 years after its establishment, and based on the extensive experience and deep familiarity with the industry, Bioforum expanded to become a service providing company in the areas of clinical data, regulatory submission and clinical supply, in addition to its core services in training and education. Our Education & Training department provides applicable knowledge and skills through education and training programs offered as either frontal or computer based (partnered with EduNeering), other services include: expert consultation, outsourcing, translation and localization. The Clinical Data team offers a complete range of clinical data management, biostatistics, data analysis and reporting solutions, from early planning to reporting and published results. In the Regulatory Submissions area we prepare, publish and compile paper & electronic submissions to agencies worldwide, providing full CTD/eCTD and regulatory submission services supporting the product development process. The GMP certified Clinical Supply plant (- inPACK) with QP services for Clinical Batch Release, specializes in contract packaging, storage and distribution solutions for all clinical trial phases and types. Our strategic lines of business combine professionals, processes, technology and education to provide complete capabilities to our clients. Throughout our services we maintain a high level quality system and adhere to all required industry standards and regulations.
