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Innovation That Shapes Global Healthcare.

Research & Development Center

Aidotick Pharmaceuticals is driven by science-led innovation. Our R&D alignment focuses on developing formulations that are stable, effective, and tailored to the needs of emerging and established markets.

With access to advanced analytical tools and experienced formulation scientists, we continuously enhance our product pipeline while ensuring compliance with international regulatory frameworks.

01

Formulation Development

Designing stable and effective formulations across multiple dosage forms.

02

Market-Specific Adaptations

Country-wise customization of packaging, strength, and dosage preferences.

03

Analytical Method Development

Precision-validated methods ensuring accurate and reliable testing.

04

Stability Studies

Climate-zone specific (Zone II, III, IV) stability testing as per ICH guidelines.

05

Packaging Optimization

Developing packaging that enhances product shelf life, patient compliance, and regulatory acceptance.

06

Regulatory-Ready Data Generation

Creating documentation that aligns with CTD/ACTD requirements for global submissions.

Innovation Commitment

Every new formulation undergoes rigorous testing and validation to ensure it meets the highest standards of safety, efficacy, and stability. Our scientific ecosystem ensures continuous technology upgrades and data-driven improvements.

Technology & Infrastructure

Scientific Innovation with Purpose. Formulations Built for Global Needs.

R&D & FORMULATION DEVELOPMENT

Needs (~900–1,000 words)

R&D & Formulation Development

Transforming Healthcare Challenges Into Safe, Effective, and Relevant Therapeutic Solutions.

Aidotick’s Research & Development approach is rooted in one belief:
Innovation must be purposeful.

Our R&D strategy aligns scientific rigor with real-world healthcare challenges across emerging and established markets.
Every new formulation we develop is guided by:

A Distributed R&D Model

A Distributed R&D Model

Aidotick collaborates with advanced formulation development centers and scientific teams aligned with WHO-GMP manufacturing facilities, ensuring a unified approach to:

This model allows us to leverage specialized expertise while maintaining global quality and regulatory consistency.

Areas of Scientific Focus

1. Generic Formulations

Optimized for quality, equivalence, and therapeutic performance.

2. Market-Specific Adaptations

Adjusting formulations to meet climatic, stability, or regulatory requirements of different countries.

3. Pediatric & Geriatric Solutions

Developing patient-friendly formats such as dispersibles, flavored syrups, and low-dose variants.

4. High-Demand Therapeutic Segments

Including:

5. Value-Engineered Products

Designed for affordability without compromising pharmacopoeial compliance.

A Distributed R&D Model

Formulation Development Capabilities

Aidotick’s formulation teams work on:

Pre-Formulation Studies
Formulation Trials
Analytical Development

Pilot Batches
Supporting scale-up for commercial production.

Stability Studies
Conducted under ICH and Zone IV conditions.

R&D Aligned With Regulatory Expectations

R&D Aligned With Regulatory Expectations

All formulations are developed with dossier readiness in mind, ensuring:

This approach ensures faster registrations and smoother market entry for partners worldwide.

Innovation at Aidotick is not about complexity — it is about creating solutions that enhance accessibility, affordability, and therapeutic impact.

Our R&D capabilities ensure that our partners receive products engineered for global relevance and regulatory excellence.

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