Pharmaceutical Industry

We solve problems, scale operations, and drive outcomes.

Understanding the Challenge

Pharmaceutical companies operate in one of the most regulated, quality-sensitive, and innovation-driven industries in the world. From formulation labs to full-scale production, they must ensure speed, safety, compliance, and traceability—without compromising quality or control. However, achieving this is easier said than done.

Formulation development is often delayed due to disconnected tools and lack of integration between R&D, QA/QC, and manufacturing. Manual documentation slows batch approvals and complicates compliance. Critical data—ranging from raw material specs to cost and yield insights—is scattered across spreadsheets and legacy systems. This limits visibility, increases the risk of regulatory violations, and reduces operational agility.

Common challenges include

These inefficiencies can lead to delayed approvals, failed audits, and increased production costs. Watern Technologies solves these challenges with a unified, intelligent platform that streamlines pharmaceutical R&D, automates compliance workflows, and enables real-time process monitoring.

What We Provide

Our Offering for your Industry

Design, test, and manage multiple formula versions with batch scalability

Generate SDS, COA, TDS, audit logs, and global compliance reports

Analyze cost, waste, and production yield by formulation and line

Monitor test results, deviations, and approval cycles in real time

Maintain full traceability and substitution logic

Match ingredients against regulatory databases (GHS, FDA, EU, etc.)

Our Approach to Solving It

Watern empowers pharmaceutical R&D and manufacturing teams with a robust platform that seamlessly integrates digital formulation tools, regulatory automation, and real-time data intelligence. Our solution dramatically enhances speed, control, and transparency across the entire drug development and production lifecycle, ensuring that teams can innovate and deliver results with confidence.

Measurable Impact with Predictive Intelligence

30–50% Faster formulation-to-production transfer

70–80% reduction in manual documentation workload

100% digital traceability from R&D to QA to manufacturing

Reduced compliance risk and faster audit readiness

Our Approach to Solving It

Here’s how we tackle your pain points

1. Digitized Formulation & Version Control

Our Process R&D Formulator allows teams to create, modify, version, and compare formulations with built-in concentration logic and unit conversions. Maintain an accurate digital trail of every formula iteration.

2. Automated Compliance & Documentation

Auto-generate SDS, COA, TDS, and batch manufacturing records. Track raw material restrictions across global compliance databases like GHS, FDA, and EU-REACH—reducing audit risk.

3. Lab to Plant Scale-Up

Seamlessly scale lab formulations to commercial batch sizes using intelligent batch calculators and transfer protocols. Integrated QA/QC checks ensure consistency during pilot and production stages.

4. Cost & Yield Optimization

Real-time visibility into material cost, labor impact, formulation wastage, and yield variance empowers better pricing, planning, and margin decisions.

5. Raw Material & Vendor Intelligence

Centralized material library with vendor specs, pricing, and availability. Suggest alternatives during shortages and flag non-compliant or high-risk ingredients.

6. Quality & Deviation Tracking

Track quality performance across batches, identify recurring deviations, and generate real-time alerts to reduce rework, recalls, and compliance breaches.

Pharma Segments We Serve

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Partner with Us for Comprehensive Solution

We’re happy to answer any questions you may have and help you determine which of our services best fit your needs.

Your benefits:
What happens next?
1

We Schedule a call at your convenience 

2

We do a discovery and consulting meeting 

3

We prepare a proposal 

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