Consultpharm
ConsultPharm is a company specializing in regulatory affairs, quality assurance, pharmacovigilance, and related services for the pharmaceutical industry. They provide expert consulting to help businesses grow and comply with industry standards.
Industries
Nr. of Employees
small (1-50)
Consultpharm
Services
Advisory and hands-on support for regulatory strategy, dossier preparation and submissions to health authorities.
Development and implementation of QA systems, SOPs and periodic quality reviews to support compliance.
Safety surveillance, adverse event reporting and compliance support with drug safety legislation.
Structured GMP audits of manufacturing operations and compliance assessments to identify regulatory gaps.
Targeted due diligence reviews addressing manufacturing, quality and regulatory risks for transactions or partnerships.
Short-duration, focused consultations for immediate regulatory or quality questions.
Advisory and hands-on support for regulatory strategy, dossier preparation and submissions to health authorities.
Development and implementation of QA systems, SOPs and periodic quality reviews to support compliance.
Safety surveillance, adverse event reporting and compliance support with drug safety legislation.
Structured GMP audits of manufacturing operations and compliance assessments to identify regulatory gaps.
Targeted due diligence reviews addressing manufacturing, quality and regulatory risks for transactions or partnerships.
Short-duration, focused consultations for immediate regulatory or quality questions.
Expertise Areas
- Regulatory compliance and submissions
- Quality assurance and quality management systems (QMS)
- Pharmacovigilance and drug safety
- GMP auditing and manufacturing compliance
Key Technologies
- Quality management systems (QMS) implementation
- GMP auditing methodologies
- Regulatory dossier preparation and submission processes
- Pharmacovigilance systems and adverse event reporting workflows
News & Updates
ConsultPharm participated in the GMP update event in Montreal on September 20-21, 2011.
ConsultPharm introduced a new due diligence service in August 2012.
ConsultPharm conducted three GMP audits within a month in November 2012.
Updated labeling requirements for non-prescription drugs and natural health products.
Introduction of a new policy regarding homeopathic products.
Updated GMP standards and guidelines.
ConsultPharm participated in the GMP update event in Montreal on September 20-21, 2011.
ConsultPharm introduced a new due diligence service in August 2012.
ConsultPharm conducted three GMP audits within a month in November 2012.
Updated labeling requirements for non-prescription drugs and natural health products.
Introduction of a new policy regarding homeopathic products.
Updated GMP standards and guidelines.