A vendor organization which doesn't only provide plain vanilla offerings but should be one stop shop for maximum of its requirement. That is how "PWS" came in existence.
PWS is a Service Provider focused on serving our clients to achieve their strategic and tactical IT Solutions & Pharma goals, and improve their competitive position, through the practices of Pharmacokinetics, Pharmacovigilance, Medical Reviewing, Testing and Maintenance, Quality Assurance, Performance Engineering & System Integration.
PWS offers specialize services in Regulatory Compliance and Quality Assurance, Quality Consulting to the Medical Devices, Biotechnology, Food and FMCG companies. We provide value-added customized solutions, processes and enhanced quality standards to optimize business process efficiencies and minimize regulatory risk.
Our experienced team of regulatory affairs service providers have knowledge and expertise that spans all types of products—from traditional pharmaceuticals, generics manufacturers, cosmetics, vaccines, biologics/biosimilars and other advanced therapies—our regulatory consulting service experts offer broad strategic knowledge that delivers an active regulatory agency network giving local coverage in global markets. That coverage enables us to apply up-to-date, robust regulatory intelligence to product-development and registration strategies.
Managing the task flow of Life Science backbone like data analysis, programming skills.
Regulatory affairs officers act as a link between companies and regulatory authorities, ensuring that products are manufactured and distributed in compliance with appropriate legislation.
Clinical data management (CDM) is a critical process in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials.
The research focus is shifting toward the use of data generated from platforms outside the conventional framework such as electronic medical records, biomedical literature, and patient-reported data in health forums.
“Securing the Manufacturing Environment Using Biometrics” tag line has to be followed and makes the Pharma-World more secure.
Assuring the expected product efficiency using various methods, keeping facts that all damage is grounded to “Zero”.
We are a young, tech-geeks dedicated to help you develop your research using optimized up to all square edge technology so that you can scale up your productivity, performance at a minimal cost which is easilyconfigured and Secured.
Our Laboratory Information Management Software, “ShawLIMS”is designed on cloud-based technology that requires no physical infrastructure. Such environment helps Scientists to focus on their research and innovation so that managing a centralized system is the least of your worries with seamless and integrated workflows.
Our objective is to improve research organizations, be it large or small, to organize their data and communicate effectively to meet their daily operational goals. ShawLIMS offers a complete solution, meeting FDA & HIPAA guidelines, including 21 CFR part 11 protocols, for individual labs in biotech, biobanks, and pharma world.
In addition to reduced costs for Shaw Laboratory Systems, there are other additional benefits to upgrading your scientific data and applications to the cloud:
Industry Training is defined as a learning process that involves the acquisition of knowledge, sharpening of skills, concepts, rules, or changing of attitudes and behaviors to enhance the performance of individuals at their immediate workplace.
© 2020 PWShaw.
