Let’s Craft the Future of Pharma with Our Collaborative Expertise
GVB is committed to driving pharmaceutical progress through the power of collaboration and expertise. The future of healthcare lies in innovative pharmaceutical solutions. To achieve this, now is the right time to connect. Together, we can revolutionise pharmaceutical advancements, improve patient outcomes, and create a more sustainable healthcare system. Our robust drug discovery and development team is ready to provide support, expertise, collaboration, and customization services tailored to our clients’ specific requirements. It’s the ultimate time to shape the future of medicine and craft a brighter and healthier world.
Partnerships with Leading API Suppliers and Trading Division
We have secured exclusive distribution agreements with renowned manufacturers in the industry, enabling us to establish a prominent presence in the API distribution business. Our extensive knowledge and expertise in the API field and our vast network of contacts have been instrumental in our success.
Our distribution operations have been a cornerstone of our company since its inception, playing a pivotal role in our current position as a leader in API distribution and the development of pharmaceutical products, which includes:
- APIs (Pharmaceuticals/Biopharmaceuticals all segments including oncology APIs)
- Vitamins
- Collagen (from veg, fish, bovine)
- Enzymes
- Pellets (blended as well as single molecules)
- Probiotics (Special blends as required)
- Herbal extracts
- Amino acids
- Nutraceutical materials (food grade/drug grade)
Our team is highly skilled in delivering Active Pharmaceutical Ingredients (API) products to Domestic and International markets, which includes Excipients, Flavours, Coating materials, Solvents and specific requirements, if any, providing comprehensive and end-to-end services to ensure timely transportation of items, with competitive rates from our supplier’s facilities to our clients’ sites.
GVB supports new vendor evaluation and sample requests based on order confirmations with technical/regulatory documentation for APIs and their reference/impurity standards.We expand our essential services in the following areas too.
- Lab Chemical Requirements
- Lab Instruments Requirements
- Machinery Spares Requirements
- Water Treatment plant chemicals and services
The Need for Collaboration
The pharmaceutical industry faces complex regulations and high development costs. As a result, drug manufacturers are increasingly turning to contract development and manufacturing organisations (CDMOs) for their in-human trials or product launches. However, finding the right outsourcing partner can be difficult. This is where a GVB life sciences consultant can help. With extensive knowledge and a vast network of CDMO contacts, consultants can help their clients find a good fit and reap significant benefits.
Our Expertise in Drug Discovery and Development
GVB life sciences consultants play a crucial role in working with CDMOs. Once key issues are addressed, they assess resource requirements, budgets, capacity, and timelines. For clients new to CDMOs, understanding the optimal relationship and outcome is essential. Previous experience plays a critical role in consultant recommendations from a partnering organization. Collaboration between the client, CDMO, and consultant is necessary for success. Having a single point of contact at the CDMO is critical. Providing vital information such as company history, experience, process costs, timelines, technical capability, and regulatory and quality issues is important.
A three-way CDA is often arranged that requires the consultant to simplify processes for their clients. Regular communication and documentation are essential. The GVB life sciences consultant acts as an extension of the client, and the CDMO should be thought of as an extension of the client’s goals. Consultants help navigate complex global requirements and provide assistance with manufacturing strategies and plans.
GVB Consultants as Client Extensions
GVB life sciences consultants are in a unique position to deal with a variety of companies and projects, allowing them to stay abreast of regulatory and quality requirements, emerging technology trends, and critical issues that affect their clients. Consultants must be knowledgeable and up-to-date to provide the best service to their clients.
We have implemented various logistics models that can be expertly customized to meet the specific needs of individual products and customers. This approach has proven a successful strategy, providing unparalleled reliability to our clients.We work flexible with our partners to give you coverage for the entire range of pharmaceutical activities, from development to promotion. We offer a variety of services to our customers, including:
- API sourcing
- Development and Manufacturing
- Quality assurance
- Regulatory compliance
- Consulting Services
- Tailored Solutions
GVB Life Sciences is committed to fostering collaborative relationships that extend beyond distribution. Provided customer requirements are satisfied, we are willing to venture outside the established distribution model and pursue innovative models to achieve our objectives. Our track record demonstrates our capacity to engage in two such collaborative efforts:
1. Development of Drug Master Files (DMF) coupled with the qualification of manufacturers for regulated markets;
2. Co-development agreements with API manufacturers aimed at advancing API development.
At GVB Lifesciences, we prioritize customer satisfaction through service and flexibility. Our experienced professionals offer partnership models tailored to meet unique needs at any project stage. We believe in solid relationships, exceptional service, and being a trusted partner throughout our client’s journey.
