Centre For Regulatory Affairs

About

CENTRE FOR REGULATORY AFFAIRS

The Centre of Regulatory Affairs (CRA) at Institute of Applied Research & Innovation serves as the hub for pioneering research, innovation, and excellence across various specialized fields. Our department is tasked with the oversight and support of multiple Centers of Excellence within the institute, ensuring that each center adheres to stringent regulatory and compliance standards. By maintaining a cohesive and rigorous approach to governance, we are dedicated to upholding the highest levels of integrity, quality, and scientific rigor.

Dr. Anand Babu Vangala
Director Centre Regulatory Affairs

Dr Anand Babu Vangala is the Director of the Centre for Regulatory Affairs at InARI. With a wealth of experience in regulatory compliance and policy, Dr. Anand ensures that all research and development activities meet stringent national and international standards. His leadership is crucial in navigating the complex regulatory landscape, facilitating innovation, and ensuring the integrity of InARI’s scientific endeavours.

VISION

To be a good global leader in advancing scientific knowledge and innovation through the establishment and governance of world-class centers of excellence.

MISSION

To support and oversee the operations of our centers of excellence ensuring they meet regulatory and compliance standards, foster interdisciplinary collaboration, and drive impactful research and development.

responsibilities

CRA Responsibilities

The Centre of Regulatory Affairs is a pivotal component within Centres of Excellence (CoEs), playing a crucial role in ensuring the success and sustainability of innovative research and development activities. The CRA is indispensable for the success of Centres of Excellence. It ensures compliance, mitigates risks, facilitates innovation, enhances global competitiveness, and supports the commercialization process, ultimately contributing to the overall mission of advancing research and development for societal benefit.

The Centre of Regulatory Affairs ensures that all research and development activities within the CoEs comply with national and international regulations and standards. This compliance is vital for maintaining the integrity and credibility of the research outputs and for ensuring that products and technologies meet safety and efficacy requirements.

Navigating the complex landscape of regulatory approvals can be challenging. The Centre of Regulatory Affairs provides expertise and guidance to streamline the approval process for new products and technologies. This reduces time-to-market and helps avoid costly delays, enabling faster access to critical innovations.

By staying abreast of regulatory changes and emerging trends, the Centre of Regulatory Affairs helps CoEs proactively manage risks. This includes identifying potential regulatory hurdles early in the development process and implementing strategies to mitigate these risks, ensuring smoother project execution.

Regulatory affairs professionals work closely with researchers and developers to understand the regulatory implications of their work. This collaboration fosters an environment where innovation can thrive within the boundaries of regulatory frameworks, encouraging the development of cutting-edge technologies and solutions.

Compliance with international regulatory standards is essential for global market access. The Centre of Regulatory Affairs ensures that the CoEs' products and technologies are compliant with these standards, enhancing their competitiveness in the global market and opening up opportunities for international collaborations and partnerships.

Adhering to regulatory standards and achieving necessary approvals build trust and credibility with stakeholders, including investors, partners, and consumers. The Centre of Regulatory Affairs ensures that CoEs maintain high standards of quality and safety, reinforcing their reputation as leaders in their respective fields.

The journey from lab to market involves numerous regulatory checkpoints. The Centre of Regulatory Affairs provides critical support for the commercialization process by ensuring that all regulatory requirements are met, facilitating the transition from research to market- ready products.

The Centre of Regulatory Affairs also plays a key role in educating and training researchers and developers on regulatory requirements and best practices. This knowledge transfer is essential for fostering a culture of compliance and awareness within the CoEs, ensuring ongoing adherence to regulatory standards.

clinical research

regulatory compliance

biobanking

audit & inspection

ethics & integrity

Diagnostics

medtech

training & education

policy development

agritech

data protection

envi genomics

CRA

regulatory compliance

ethics & integrity

policy development

data protection

training & education

audit & inspection

clinical research

biobanking

Diagnostics

agritech

envi genomics

medtech

Collaboration and Innovation

The CRA fosters a culture of collaboration and innovation by

Establishing innovation hubs to support the development of new ideas and technologies. These hubs provide a collaborative environment for researchers to explore new concepts.

Encouraging collaboration between different Centers of Excellence and external partners. This includes joint research projects and interdisciplinary teams.

Organizing seminars, workshops, and conferences to share knowledge and best practices. These events provide opportunities for researchers to learn from each other and from experts in their fields.