PharmInstinct
Consultancy providing technical and quality-focused support across pharmaceutical product development, manufacturing, testing and project management. Offers formulation and process development, technology transfer, QA/QC and regulatory compliance consulting to pharmaceutical organizations, with on-site and remote delivery.
Industries
Nr. of Employees
small (1-50)
PharmInstinct
Services the Greater Toronto Area, Ontario, Canada; also available online, by phone and video conference internationally.
Services
Consulting on design and development of solid, liquid and parenteral formulations.
Development and optimization of manufacturing processes and supporting scale-up to pilot or commercial production.
Planning and managing technology transfer activities and serving as liaison with CDMOs to ensure robust transfer and manufacturing capability at receiving sites.
QA/QC system development, GMP/GLP compliance auditing and CMC QA review for clinical trial materials.
Project coordination and leadership for multidisciplinary teams across development and manufacturing projects.
Consulting on design and development of solid, liquid and parenteral formulations.
Development and optimization of manufacturing processes and supporting scale-up to pilot or commercial production.
Planning and managing technology transfer activities and serving as liaison with CDMOs to ensure robust transfer and manufacturing capability at receiving sites.
QA/QC system development, GMP/GLP compliance auditing and CMC QA review for clinical trial materials.
Project coordination and leadership for multidisciplinary teams across development and manufacturing projects.
Expertise Areas
- Formulation development (solid, liquid, parenteral)
- Manufacturing process development and scale-up
- Technology transfer and inter-site transfer
- Quality assurance and quality control
Key Technologies
- Formulation science for solid and liquid dosage forms
- Parenteral product development
- Design of Experiments (DoE)
- Quality by Design (QbD) methodologies
News & Updates
Discussion of identifying Critical Process Parameters (CPPs) early in formulation development, and using Critical Quality Attributes and Design of Experiments to support robust process design and technology transfer.
Discussion of identifying Critical Process Parameters (CPPs) early in formulation development, and using Critical Quality Attributes and Design of Experiments to support robust process design and technology transfer.