Training, Consulting & Problem Solving
Our approach
From formulation to validation, with a QbD approach
PPI supports pharmaceutical and biotech teams across the full development journey — from formulation and process design to process characterization and validation — using a Quality by Design (QbD) approach, grounded in first-principles science.
Core service pillars
Three pillars of service
Advanced Training & Capability Building
We deliver high-level workshops and seminars designed for professionals in the pharmaceutical and biotech industries.
Our training bridges the gap between academic theory and the daily realities of the cleanroom, focusing on modernizing lyophilization processes and optimizing equipment performance.
Strategic Consulting and Advisory
We provide comprehensive, high-level guidance for pharmaceutical manufacturing projects.
Whether you are navigating complex scale-up strategies or seeking to optimize your existing process lines, we provide the technical roadmap required to ensure regulatory excellence and operational success.
Technical Problem Solving
Facing persistent manufacturing bottlenecks?
We offer specialized technical troubleshooting for complex production challenges.
By utilizing a deep analytical approach, we help teams resolve performance issues, improve throughput, and maintain the highest standards of aseptic processing.
Process development
From formulation & process design to characterization & validation
Using a Quality by Design (QbD) approach, grounded in first-principles science.
Fields of Expertise (Technical Depth)
From formulation & process design to characterization & validation
Particle Engineering & solid dosage forms
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Particle Engineering & solid dosage forms
- Mechanical milling, jet milling, nanomilling
- Spray drying, drum drying
- Amorphization
- Powder mixing, fluid-bed drying
- Wet granulation, dry compaction, compression
- Coating, microspheres
Parenteral — Fill & Finish & Lyophilization
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Parenteral — Fill & Finish & Lyophilization
- Formulation, freezing & thawing
- Homogenization, sterile filtration
- Filling of primary containers, stoppering, capping
- Freeze drying (lyophilization)
- Functional analysis for syringes
- Container closure integrity testing (CCIT)
Nanomedicine & Advanced Drug Delivery Systems
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Nanomedicine & Advanced Drug Delivery Systems
- Emulsions, liposomes
- Lipid nanoparticles (LNPs)
- Nanocrystalline suspensions
- Polymeric nanoparticles
- Colloidal science
Technological Project & Technology Engineering
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Technological Project & Technology Engineering
- Needs & objectives definition
- Risk analysis
- User Requirement Specifications (URS)
- Calls for quotation & supplier selection
- Analysis & alignment of quotations
- FAT / SAT follow-up
De-risk industrialization
Reduce development and industrialization risk
Independent, confidential and pedagogy-focused support — from pilot to commercial scale.
What makes PPI different
PPI combines deep scientific expertise with extensive industrial experience
Typical Engagements
- Early-stage development strategy definition
- Process design, optimization & robustness assessment
- Troubleshooting and issue resolution
- Technology transfer and scale-up support
- Support to pilot, commercial & CDMO environments
Training Audience
- Process development scientists
- CMC teams
- MSAT engineers
- Tech transfer leaders
- CDMO technical teams
- Students from academic institutions
Consulting Audience
- Biotech companies (early to late clinical)
- CDMOs seeking process robustness & harmonization
- Pharma companies needing independent technical assessment
Let's work together
Let's build robust development together
Independent and strictly confidential.