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Aadhya DMF-Dossier & Export Services

Welcome To Aadhya DMF-Dossier & Export Services

A Strategic partner navigating safety in life sciences with global insights.

Slide 1
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Aadhya DMF-Dossier & Export Services

Welcome To Aadhya DMF-Dossier & Export Service​s

A Strategic partner navigating safety in life sciences with global insights.

ABOUT

Aadhya DMF-Dossier & Export Services (ADMFES)

From development to market access, we help companies of all sizes ensure that their development plans are designed and implemented for regulatory approval and market access.

With us as your partner, you’ll benefit from step-by-step guidance on compliance, documentation, and regulatory engagement at every phase. Our priority is helping your team avoid delays, meet standards, and confidently bring your innovative products to customers.

Let’s take the hassle out of approvals, so you can focus on growing your big ideas

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SERVICES TAILORED TO FIT ALL YOUR NEEDS

Regulatory Affairs

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ADMFES is dedicated to guiding clients through global regulatory landscapes with streamlined, accelerated, and cost-effective services that ensure compliance and success throughout product development and lifecycle.

Pharmacovigilance, MICC& PSP
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ADMFES provides expert pharmacovigilance solutions, offering comprehensive drug safety services and a 24/7 Medical Information Call Center, enhancing therapy adherence and improving treatment outcomes through close collaboration

Clinical Trial

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ADMFES is here to help you navigate clinical trials smoothly. Our knowledgeable team offers supportive, expert guidance and management to make your trial journey efficient, compliant, and successful.

TENDER FILLING

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ADMFES specializes in tender filling for pharmaceutical medicines, offering expert preparation, regulatory compliance, and submission services to enhance clients’ success in competitive procurement processes.

Medical Device

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ADMFES offers expert support for FDA and CDSCO medical device dossier filling, ensuring comprehensive regulatory compliance, accurate documentation, and timely submissions for smooth approvals in markets.

Post-Approval LCM

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ADMFES supports post-approval lifecycle management by managing regulatory changes, renewals, and compliance. It helps overcome re-registration difficulties through expert regulatory submissions and strategy to maintain product approval.

Product Development & Testing

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ADMFES offers product development and testing with advanced in-house laboratories, ensuring high quality through analytical method development (AMVs) and robust testing to support regulatory compliance

Market Entry

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ADMFES excels in supporting global clients to successfully enter international pharmaceutical markets, helping them establish strong presence and thrive by navigating regulatory, marketing, and compliance challenges efficiently.

Our Clients

Trusted by visionary clients who drive innovation and success together with us.

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Our Clients’ Journey

Bringing life sciences solutions under one roof, committed to your growth and success.

"Thanks to Admfes, our first international regulatory dossier was completed ahead of schedule. Their expertise in aligning technical data with tender specifications saved time and resources. Their professionalism and precision have been invaluable to our successful regulatory submissions."

— Mrs. Ruby, MD

Medyra Pharmaceutical, Delhi

"ANG Lifesciences relies on Admfes for precise dossier preparation and timely submissions. Their expertise in regulatory compliance has significantly enhanced our operational efficiency, ensuring successful market entries and tender wins. Their professionalism and attention to detail make them an invaluable partner in our growth journey."

— Mrs. Sudesh,

ANG Lifesciences, Punjab & HP

"Aveo Pharmaceutical Ltd. has relied on Admfes for expert guidance in navigating the complex regulatory landscape of pharmaceutical and nutraceutical product registration in Tajikistan. Admfes stands out as a trusted partner for regulatory success in challenging and evolving markets."

— Mr. Ajay, MD

Aveo Pharmaceutical Ltd., Mumbai

"Under Admfes' expert guidance, K R Pharma successfully submitted dossiers in Tajikistan, Nepal, and Afghanistan. Their mastery of regulatory documentation and local compliance ensured smooth, timely approvals. Admfes’ professionalism and diligence have been key to our growth in these challenging markets."

— Mr. Rahul, MD,

K R Pharma, Uttar Pradesh

"Admfes has been an exceptional regulatory partner. Their deep understanding of global dossier requirements especially (AMV), documentation, and export compliance ensured our submissions were precise, efficient, and timely. Their proactive approach and technical clarity make them a trusted extension of our R&D operations."

— Mr. Mahesh Bharati,

R&D Head, Aishwarya Life Sciences Group

Call Aadhya DMF-Dossier & Export Services Now

+(91) 96462 79546

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