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- info@pharmaffairs.in
About Us
About Us
Who We Are
KP Pharmaffairs is a leading Pharmaceutical Project Consulting company in India that is well known for providing one-stop Solutions to Finished Formulations, Nutraceuticals, Cosmetics, Ayurvedic, Bulk Drug, KSM’s, Commercial testing labs and R&D, F&D sectors With Profound Experience and specialization in greenfield projects, turnkey solutions, Facility Upgradation and Expansion, Regulatory Compliance, Drug Regulatory Affairs, External Audit, Product Stability Assessment and other Third Party Services. Blend of innovation and technology with knowledge bank of prevailing regulatory norms is led by Mr. Kapil Dhiman, who has over 30 years of experience in drug regulation and has passion for consulting and has set up over 100 green field and expansion projects in Himachal Pradesh which is considered as Asia’s biggest pharmaceutical industrial hub. At KP Pharmaffairs we are more than consultants, our experts are devoted in providing assistance with the most intricate pharmaceutical projects as though these were our own. Alongside assisting in setting up new manufacturing facilities, our vast experience in consulting of over three decades helps us to provide complete pharmaceutical project consultancy services in compliance Indian (cGMP) and Global Regulatory requisites (WHO-GMP, USFDA, EUGMP, MHRA, TGA)
We are glad to introduce KP Pharmaffairs, the leading company that specializes in pharmaceutical project consultancy. Our firm is well known for sophisticated greenfield projects and turnkey solutions with the depth understanding in drug regulatory compliance. We excel in helping clients undertake extensive processes in pharmaceutical and allied industries and are capable in implementing both Indian and international regulations. We proudly help enhance the functioning of pharmaceutical and allied industries and businesses across the globe.
Why Us
We helping your business build and grow
Deep Regulatory Expertise
With extensive experience serving as a drug regulatory authority, we offer unparalleled expertise in navigating complex regulatory landscapes. Clients can benefit from your insider knowledge of regulatory processes, requirements, and expectations, giving them a significant advantage in gaining approvals and ensuring compliance.
Holistic Understanding
Over decades-long experience provides you with a holistic understanding of the pharmaceutical industry, encompassing not only regulatory aspects but also technical, scientific, and commercial considerations. Clients can rely on your comprehensive expertise to address multifaceted challenges and optimize their overall project outcomes.
Strategic Guidance
Beyond regulatory compliance, you can offer strategic guidance to clients based on your in-depth understanding of industry dynamics, market trends, and competitive landscapes. Clients can benefit from your strategic insights to make informed decisions, optimize resource allocation, and maximize opportunities for success.
Tailored Solutions
Leveraging our wealth of experience, we can offer tailored solutions that are specifically aligned with each client's unique needs, goals, and challenges. Clients can expect personalized attention and bespoke strategies that address their specific circumstances, ensuring optimal outcomes and satisfaction.
Risk Mitigation
Drawing on their wealth of experience, the founders can help clients identify and mitigate regulatory risks associated with their projects. By proactively addressing potential pitfalls and compliance issues, the company helps clients minimize disruptions and maximize the likelihood of success.
Continued Learning and Adaptation
Despite their extensive experience, the founders understand the importance of staying abreast of evolving regulations and industry trends. As such, the company is committed to continuous learning and adaptation, ensuring that clients benefit from the latest insights and best practices in drug regulatory affairs.
Ready to turn dreams into reality? Let's get started now!
Start your journey toward achieving project excellence with KP Pharmaffairs. Let’s work together to transform the future of pharmaceutical development and take the leap together.
Our Vision
“To be a globally recognized leader in pharmaceutical project consulting, driving innovation, efficiency, regulatory adherence and excellence by delivering of cutting-edge solutions that transform the industry and improve global healthcare outcomes.”
Our Mission
Core Values
It is our policy to dedicate ourselves to customers’ success. We make sure our services address their specific needs which enhances their success.
We ensure that the pharmaceuticals industry projects are compliant with all regulatory prerequisites. It is our responsibility to ensure our clients’ endeavours exceed industry regulations.
In pursuit of delivering quality and innovative solutions beyond expectations, we set new industry standards while expecting nothing less from ourselves. We are committed to excellence in our work and continuously improve policies and procedures in place.
Through constant engagement with clients and within our company, we integrate various ideas and expertise to take on intricate pharmaceutical problems head on. We foster collaboration through and through.
Creativity while using new technologies is a strong focus for us as we attempt to stay ahead of the trends within our industry. We encourage out-the-box thinking as it allows for the development of new solutions for clients.
All interactions, regardless of who they are with, are conducted in a transparent manner and devoid of any misleading actions. Clients, employees, and other stakeholders are able to put their trust in our ethical standards because we are accountable to delivering our promises.
Our Team
Leadership Team
Kapil Dhiman
Founder
His career spanning three decades makes Kapil Dhiman an equally qualified professional in the pharmaceutical domain. He is a holder of B. Pharm (BIT) and MBA and kicked off his career as a dynamic Drugs Regulator, which gives him exceptional skills in regulatory frameworks and compliance. Having spent 30 years in this regulatory role, he came out well versed with trends of the industry and developed quality, safety, and ethical practice concerns regarding the pharmaceutical industry.