Global pharmaceutical manufacturing facility

30+

Countries

25+

UNIQUE DOSAGE FORMS

20+

MANUFACTURING PARTNERS

500+

Successful
Registrations

30+

Countries

25+

UNIQUE DOSAGE FORMS

20+

MANUFACTURING PARTNERS

500+

Successful
Registrations

CORE SERVICES

Launch Market-Winners

We help you pick the right products, craft a standout formula, and move it from idea to warehouse in no time.

pharmaceutical product launch strategy, rapid formulation development, pharma market entry services

Launch Market-Winners

We help you pick the right products, craft a standout formula, and move it from idea to warehouse in no time.

pharmaceutical product launch strategy, rapid formulation development, pharma market entry services

Launch Market-Winners

We help you pick the right products, craft a standout formula, and move it from idea to warehouse in no time.

pharmaceutical product launch strategy, rapid formulation development, pharma market entry services

Ideal Quality at Ideal Pricing

Your product runs on rigorously audited GMP lines under our embedded QA crew, while cost engineering keeps every package patient friendly and margin-smart.

affordable pharmaceutical quality assurance, GMP compliance, cost-efficient pharma production

Ideal Quality at Ideal Pricing

Your product runs on rigorously audited GMP lines under our embedded QA crew, while cost engineering keeps every package patient friendly and margin-smart.

affordable pharmaceutical quality assurance, GMP compliance, cost-efficient pharma production

Ideal Quality at Ideal Pricing

Your product runs on rigorously audited GMP lines under our embedded QA crew, while cost engineering keeps every package patient friendly and margin-smart.

affordable pharmaceutical quality assurance, GMP compliance, cost-efficient pharma production

Fast-Track Your Registration

Country-tuned CTD dossiers, mock audits, and realtime query resolution strip months from approval clocks and millions from lost opportunity.

accelerated drug registration services, CTD dossiers, pharma regulatory approvals

Fast-Track Your Registration

Country-tuned CTD dossiers, mock audits, and realtime query resolution strip months from approval clocks and millions from lost opportunity.

accelerated drug registration services, CTD dossiers, pharma regulatory approvals

Fast-Track Your Registration

Country-tuned CTD dossiers, mock audits, and realtime query resolution strip months from approval clocks and millions from lost opportunity.

accelerated drug registration services, CTD dossiers, pharma regulatory approvals

Manufacturing-to-Delivery—Our Guarantee

We own production, serialisation, customs, and last-mile logistics— so the finished product arrived within the agreed upon timeline

end-to-end pharma manufacturing, serialisation, last-mile pharmaceutical logistics

Manufacturing-to-Delivery—Our Guarantee

We own production, serialisation, customs, and last-mile logistics— so the finished product arrived within the agreed upon timeline

end-to-end pharma manufacturing, serialisation, last-mile pharmaceutical logistics

Manufacturing-to-Delivery—Our Guarantee

We own production, serialisation, customs, and last-mile logistics— so the finished product arrived within the agreed upon timeline

end-to-end pharma manufacturing, serialisation, last-mile pharmaceutical logistics

STATISTICS

2M+

Packs Shipped

GDP-compliant lanes to 27 ports—zero temperature excursions.

2M+

Packs Shipped

GDP-compliant lanes to 27 ports—zero temperature excursions.

95%

On-Time Delivery

Strong supply chain principles ensure matching schedules to delivery.

95%

Satisfied Clients

Strong supply chain principles ensure matching schedules to delivery.

75+

Pharmaceuticals Professionals

QA, RA, and formulation specialists powering every batch.

75+

Pharmaceuticals Professionals

QA, RA, and formulation specialists powering every batch.

15+

New Formulations Developed

Our discovery lab turns concepts to market ready formulations

15+

New Formulations Developed

Our discovery lab turns concepts to market ready formulations

Alvita Pharma company milestones, global presence, product portfolio growth, regulatory approvals

HOW WE WORK?

pharma market analysis, product selection strategy, consultation services for pharmaceutical companies

1-2 weeks

01

Market & Product Consultation

pharma market analysis, product selection strategy, consultation services for pharmaceutical companies

1-2 weeks

01

Market & Product Consultation

pharma manufacturing partner sourcing, GMP facility identification, supply chain setup

2-3 weeks

02

Manufacturing Partner Selection

pharmaceutical branding, packaging design, product finalization process

1-2 weeks

03

Brand Development & Finalization

regulatory dossier documentation, pharma compliance submission, CTD preparation

1-2 months

04

Dossier Preparation & Submission

1-2 months

04

Dossier Preparation & Submission

drug launch process, pharma market authorization, regulatory approvals for medicines

2-12 months

05

Market Authorization & Launch

2-12 months

05

Market Authorization & Launch

FAQs

(Frequently asked questions)

Minimum Order Quantity (MOQ)

We keep MOQ flexible—small validation batches for market entry and the capacity to scale to multi-million lots once demand takes off.

Minimum Order Quantity (MOQ)

We keep MOQ flexible—small validation batches for market entry and the capacity to scale to multi-million lots once demand takes off.

Certifications Your Plants Hold

Novagen holds PICS- and WHO-GMP certifications, with partner access to EU GMP, US FDA, ANVISA (Brazil), and MHRA (UK) approvals to match each SKU with your market’s exact requirements.

Certifications Your Plants Hold

Novagen holds PICS- and WHO-GMP certifications, with partner access to EU GMP, US FDA, ANVISA (Brazil), and MHRA (UK) approvals to match each SKU with your market’s exact requirements.

Co-Develop a New Formulation

Yes. Our R-&-D centre launches 15 + new formulations a year and offers milestone-based co-development—shared IP or full tech transfer, depending on your preference.

Co-Develop a New Formulation

Yes. Our R-&-D centre launches 15 + new formulations a year and offers milestone-based co-development—shared IP or full tech transfer, depending on your preference.

Dedicated Order Support

Your Commercial, RA and QA leads stay on the project from dossier to post-market, replying within one business day.

Factory Audit Support

We host physical audits all year and can arrange a full virtual walk-through of any facility as per your request.

Back-Up Sites

We have pre-qualified secondary sites just in case we need to switch production - avoiding fresh registration and no supply gap

TIMELINE

Alvita Pharma founded

Incorporated in 2010, we set out to unite R&D, manufacturing, and regulatory expertise under one trusted partner.

Alvita Pharma founded

Incorporated in 2010, we set out to unite R&D, manufacturing, and regulatory expertise under one trusted partner.

Alvita Pharma founded

Incorporated in 2010, we set out to unite R&D, manufacturing, and regulatory expertise under one trusted partner.

Novagen manufacturing facility launched

Novagen plant goes live, adding WHO-GMP-grade capacity and scaling complex dosage production for global exports.

24C Derma domestic brand launched

Debut of 24C Derma channels our science into everyday skincare, anchoring a new consumer-facing vertical.

2010

2010

2012

2012

2018

2018

2020

2020

2022

2022

2024

2024

First R&D center opened

Our inaugural R&D hub accelerates formulation innovation, slashing time-to-market and giving clients a decisive edge.

First R&D center opened

Our inaugural R&D hub accelerates formulation innovation, slashing time-to-market and giving clients a decisive edge.

First R&D center opened

Our inaugural R&D hub accelerates formulation innovation, slashing time-to-market and giving clients a decisive edge.

100+ Cr turnover achieved

Crossing the ₹100 crore mark confirms that quality, reliability, and regulatory agility translate into sustained growth.

100+ Cr turnover achieved

Crossing the ₹100 crore mark confirms that quality, reliability, and regulatory agility translate into sustained growth.

100+ Cr turnover achieved

Crossing the ₹100 crore mark confirms that quality, reliability, and regulatory agility translate into sustained growth.

Team expansion to 70+ professionals

A 70-strong multidisciplinary team now blends science, compliance, and market insight to power our next decade.

Team expansion to 70+ professionals

A 70-strong multidisciplinary team now blends science, compliance, and market insight to power our next decade.

Team expansion to 70+ professionals

A 70-strong multidisciplinary team now blends science, compliance, and market insight to power our next decade.

Start your export journey today!

MUMBAI | AHMEDABAD | VADODARA

Copyright @2025 Alvita. All rights reserved

MUMBAI | AHMEDABAD | VADODARA

Copyright @2025 Alvita. All rights reserved

MUMBAI | AHMEDABAD | VADODARA

Copyright @2025 Alvita. All rights reserved