Technical & Scientific Services

Scientific excellence is the foundation of successful pharmaceutical product development. From formulation design to analytical validation and regulatory documentation, every stage must demonstrate accuracy, reproducibility, and compliance

At InPharma Solutions, we provide end-to-end technical and scientific support tailored to pharmaceutical, API, formulation, and research organizations. Our approach integrates scientific rigor with regulatory alignment — ensuring your development programs are efficient, defensible, and inspection-ready

We support innovation with compliance

Formulation Support

Developing a robust formulation requires a deep understanding of API characteristics, excipient compatibility, process feasibility, and regulatory expectations

We provide scientific support for:

• Pre-formulation studies
• Excipient compatibility studies
• Prototype formulation development
• Process optimization
• Scale-up strategy
• Technology transfer documentation
• Troubleshooting formulation challenges

Our team ensures your formulation is not only scientifically optimized but also aligned with stability, manufacturability, and regulatory requirements

We bridge R&D excellence with commercial success

Analytical Method Development & Validation

Reliable analytical methods are critical for product quality, regulatory submissions, and lifecycle management

We provide comprehensive support in:

• Method development for assay, impurities, dissolution, and related substances
• Forced degradation & stability-indicating method development
• Method optimization & robustness studies
• Analytical method validation as per ICH guidelines
• Transfer of analytical methods between laboratories
• Preparation of validation protocols & reports

Our validation approach ensures:

• Accuracy
• Precision
• Specificity
• Linearity
• Robustness
• Reproducibility

We deliver analytical confidence that withstands regulatory scrutiny

Stability Studies Support

Stability programs determine product shelf life and regulatory approval timelines

We provide support for:

• Stability protocol design (accelerated, long-term, intermediate)
• Bracketing & matrixing strategies
• Stability data review & trend analysis
• Out-of-trend evaluation
• Shelf-life justification
• Regulatory stability documentation

We ensure your stability studies are scientifically justified, statistically evaluated, and submission-ready

OOS / OOT Investigation

Out-of-Specification (OOS) and Out-of-Trend (OOT) results are critical quality events requiring structured scientific investigation

We provide:

• Phase I & Phase II investigation support
• Laboratory error assessment
• Root Cause Analysis (RCA)
• Hypothesis testing
• Data integrity review
• Impact assessment on batches
• CAPA recommendations
• Regulatory-compliant investigation reports

Our approach is objective, scientific, and fully aligned with global regulatory expectations

We ensure investigations are defensible, transparent, and inspection-ready

Study Reports & Documentation

Accurate and structured documentation is essential for regulatory submissions, internal quality assurance, and global market approvals

We support preparation and review of:

• Analytical validation reports
• Stability study reports
• Method transfer reports
• Technical evaluation reports
• Development reports
• Toxicological study summaries
• Risk assessment documentation
• Regulatory submission-ready dossiers

Our documentation reflects clarity, technical depth, and compliance alignment — ensuring smooth regulatory review and faster approvals