We offer customized, end-to-end solutions to fulfill our clients’ R&D and manufacturing needs. Alpha Omega is an integrated R&D, manufacturing, and distribution company. Because of our shared interest in science and commitment to project delivery, we are able to develop client relationships that go beyond traditional service outsourcing. Project-by-project, trust is built. Our deep, long-term client relationships underpin our business and demonstrate the value of our services.
Our team is fully committed to ensuring the success of your trials. Additionally, we share our knowledge and expertise as needed. Making informed decisions will be easier if you do this.You get a transparent view of your project, proactive communication, and a team invested in your success when you work with us. We offer an unparalleled level of collaboration and flexibility.
We empower our customers to improve human health.
Therefore, we engage the best scientific talent, adhere to the highest quality standards, and pursue innovation relentlessly. Together, we can achieve a world where every patient gets the right treatment, at the right time by accelerating and de-risking drug development.
Over the past 18 years Alpha Omega has conducted over 300+ clinical trials in a vast range of therapeutic indications. The graphs below represent the last 3 years of this experience.
*Other: Pediatrics, Dermatology / Infectious diseases, Vaccines, Gynecology / Surgery, Trauma / Surgery, General Medicine
By listening carefully, thinking freely, and taking ownership of every single project, we are transforming clinical research.
Our success depends on creating an environment where our employees feel that their ideas, opinions and contributions are valued. We value his, her, their, etc. transparency. and integrity, as well as fostering a collaborative, performance-oriented culture.
At Alpha Omega, our work is more than just a job – it’s a chance to change lives and shape the future of medicine.
We believe in the importance of effective patient recruitment starting at the grassroots level. This means choosing the right sites and working with them to maximize the potential of your listings. We work closely with them to plan and manage operations locally, from translating protocols to designing effective screening strategies to identify the right patients. This approach has resulted in an unparalleled track record in patient recruitment whereby our team has met or shortened the duration of the project in 95% of the trials conducted.
Our experienced feasibility team will quickly prepare a detailed feasibility/feasibility report. It will suggest the optimal way forward, including a country/location strategy and site selection from suggested locations.
The health of our patients is our top priority. We are fully ICH-GCP compliant and ensure that patients in our studies are well informed and have a direct line of communication with our researchers and research team . Our multilingual patient portal provides relevant educational materials about clinical trials and patient rights.
Our quality management system is based on quality-by-design principles including integrated planning, project-specific quality agreements, real-time analysis based on project risk, target monitoring based on analytical data, and customer-centric project optimization.
