Trusted by Clients in 30+ Countries,

And They Stay

Our clients don’t just work with us — they stay with us. With near-zero churn, reliable fulfillment, and proactive alliance management, Alvita is more than a service provider — we’re a partner built around your success.

WHAT WE DO,

AT A GLANCE

WHAT WE DO, AT A GLANCE

Product Strategy & Consultation

Product Strategy & Consultation

Formulation Development & R&D

Formulation Development & R&D

Manufacturing & Quality Oversight

Manufacturing & Quality Oversight

Post-Market Lifecycle Management

Post-Market Lifecycle Management

Regulatory Affairs & Registration

Regulatory Affairs & Registration

Global Commercialization Support

Global Commercialization Support

YOUR JOURNEY WITH ALVITA

From vision to education,
we walk with you at every step.

From vision to education, we walk with you at every step.

pharma brand development and lifecycle support journey
pharma brand development and lifecycle support journey
pharma brand development and lifecycle support journey

STEP-BY-STEP PARTNERSHIP MODEL

pharmaceutical market research and consultation services

1-2 weeks

01

Market & Product Consultation

100+ market consultations

delivered across emerging and established pharma regions

We start by understanding your target region, product goals, and competitive landscape. Our team evaluates therapeutic gaps, analyzes demand, and recommends product categories and dosage forms suited for regulatory approval and commercial success.

custom formulation and stability testing for pharma products

4-12 weeks

02

Formulation Development

200+ formulations developed

many now market leaders in their category

We operate a dedicated R&D center in Mumbai, reflecting our long-standing focus on innovation rather than just export. Our R&D experts design or adapt formulations based on your market requirements. We ensure technical precision through:

Custom formulation design

Custom formulation design

Stability and compatibility testing

Stability and compatibility testing

Pilot batch and bioequivalence support

Pilot batch and bioequivalence support

certified pharmaceutical manufacturing facility selection

2-4 weeks

03

Manufacturing Partner Selection

20+ certified partner facilities

managed under active oversight

Based on your product type and volume, we match you with the most suitable WHO-GMP/PICS/EU/USFDA-approved facility. Our QA/QC team remains involved throughout to ensure consistency and compliance.

pharma brand identity and packaging design strategy

2-3 weeks

04

Brand & Packaging Finalization

20+ certified partner facilities

managed under active oversight

We support brand localization, packaging compliance, and visual assets for launch. This includes label design, multilingual artwork, and local regulatory packaging formats.

pharma product quality assurance and batch testing
in-process quality control at certified facility
packaging and regulatory vetting for pharma launch
regulatory dossier preparation and submission for global markets

2-3 months

05

Dossier Preparation & Submission

1500+ dossiers

prepared and submitted across 30+ global markets

Our regulatory affairs team handles all documentation preparation and submission.

CTD, ACTD, and country-specific dossier compilation

CTD, ACTD, and country-specific dossier compilation

Country-specific adaptation and formatting

Country-specific adaptation and formatting

Regulatory query handling and updates

Regulatory query handling and updates

pharmaceutical product approval and market authorization

2-4 weeks

06

Manufacturing Partner Selection

500+ market approvals

secured with customized launch support

We track your registration status, coordinate with regulatory bodies, and manage dispatch and launch. Post-approval, we also support logistics, CDMO execution, and market readiness.

OUR RETENTION FORMULA

500+

Successful registrations

across CIS, Southeast Asia, and Africa

500+

Successful registrations

across CIS, Southeast Asia, and Africa

0%

Churn

across multi-year strategic clients

0%

Churn

across multi-year strategic clients

24/7

Successful registrations

across CIS, Southeast Asia, and Africa

24/7

Successful registrations

across CIS, Southeast Asia, and Africa

70+

Pharma professionals

dedicated to your success

70+

Pharma professionals

dedicated to your success

1

Point contact

for seamless communication

1

Point contact

for seamless communication

client collaboration and project oversight in pharma operations

WHAT CLIENTS SAY

trusted client partnerships and team collaboration in pharma

“We chose Alvita for their regulatory speed. We stayed for their follow-up, responsiveness, and ownership.”

Regulatory Head,
West Africa-based Pharma Importer

Let's build something that lasts!