The research and development (R&D) process for WELCURE REMEDIES refers to scientific and technological advancement that is aimed at improving human health and well-being. This process involves a range of activities, including:
Problem identification: The first step in the R&D process is to identify the problems or challenges that need to be addressed. This could involve identifying the health issues that affect a particular population or the lack of effective treatments for a specific disease.
Research: Once the problems have been identified, the next step is to conduct research to understand the underlying causes and mechanisms of these problems. This could involve laboratory studies, observational studies, and other types of research to gather information and data.
Development: After conducting research, the next step is to develop solutions to address the identified problems. This could involve developing new treatments, drugs, medical devices, or other types of interventions.
Testing and evaluation: Before a solution can be implemented, it must be tested and evaluated to determine its safety and efficacy. This could involve conducting animal studies, clinical trials, or other types of testing to gather data and information.
Regulatory approval: Once a solution has been tested and evaluated, it must be approved by regulatory authorities before it can be used by the public. This process involves submitting data and information to demonstrate the safety and efficacy of the solution.
Implementation: Once a solution has been approved, it can be implemented and used to improve human health and well-being. This could involve distributing drugs, medical devices, or other types of interventions to patients and healthcare providers.
The R&D process of Integrated Laboratories is an ongoing process that requires significant investment and effort. However, it has the potential to make a significant impact on human health and well-being by developing innovative solutions to improve the lives of people around the world.
The following capabilities are part of our lab’s dosage development equipment:
- Technical assistance for manufacturing.
- Development of novel, modified release Solid Oral dosage forms
- Development of drugs with poor solubility to enhance solubility and bioavailability
- Data management (for transfer to customer / Regulatory Affairs).
- Pre formulation studies.
- Technology transfer of new products.
- Scale up for process optimization / validation.
- Cost effective Test masking Technology
- Prototype Equipments as that of manufacturing facilities.
- Design and development of pharmaceutical products of International standards.
- Lab / pilot scale development and stability studies.
