Facility Design and Layouts: for traditional stainless, single use, or hybrid manufacturing platforms. :
is an important aspect of biopharmaceutical manufacturing, however critical factors such as total cost of ownership, time to market, regulatory requirements are key concerns in any manufacturing platforms - traditional stainless, single use, or hybrid manufacturing platforms. We at TAVASBIO can be your choice of partners to develop these designs and layouts to increase efficiency, productivity, and flexibility from your existing production suite or a complete new facility.

Installation & operational qualification processes
Get ready for seamless system installation and qualification with our expert team of engineers. We handle everything from system unpacking, document review, placement, consumables, spares check and more. Whether its single-use or multi-use systems, we ensure a smooth process for your manufacturing needs in upstream and downstream manufacturing layouts

Designing Implementation strategies :
As per a recent survey one of the prime factor which is a barrier for not implementing Single use systems(SUS) in manufacturing operations is lack of experience or no training to the operators on the handling, assembly and operations of these SUS. We at TAVASBIO can work with your team to provide hands on trainings on assembly, sterile connections, operations and handling these systems. This will enable your team with required skill set to confidently integrate routine manufacturing operations with SUS.

Extractable and Leachable- Developing and executing strategies and validation:
One of the primary factors restricting the adoption of Single use systems are the concerns associated with the extractable and leachable that can potentially migrate into the drug attributing to its high organic polymer content in these Single use assemblies. However a systematic approach to understanding these extractable and leachable compounds and correlating to patient safety will be a key success factor. Our TAVASBIO team of specialists from the industry with a high level of understanding on this matter can support you in developing the E & L Validation strategies.

Documentation and training support
If you are looking at outsourcing documentation activities, then at TAVASBIO our team of experienced technical specialists can support you on a numerous documentation activities including preparation of SOP's, design validation protocols and general operations guidelines.
Training of production staff and operators is the key to maintain a successful operation. At TAVASBIO we have an experienced team to support trainings on basic unit operations, process equipments (including the Bioreactors, Chromatography systems and Single use Systems).