Consultancy Services
Flexible expertise when you need it.
At Herlev Pharma Service, we are experts at quickly understanding your challenges and efficiently identifying the best solution for your organisation.
We offer two types of consultancy services tailored to support your business needs:
Ongoing and flexible support:
Tailored Consultancy Services →
Full-time consultant:
Full-Time Consultancy Services →
Tailored Consultancy Services
Herlev Pharma Service’s tailored consultancy services are available both to companies using our storage and handling services and to smaller companies that need an on-call consultant for specific assignments and quality-related guidance.
Let us help you address your challenges and identify a cost-effective solution.
We are committed to delivering tailored solutions that ensure compliance, improve processes, and support your operational objectives.
Examples of tailored consultancy services:
- Product registration with regulatory authorities (marketing authorisation)
- Establishment of quality management systems (QMS)
- Management of deviations and CAPAs, and quality management consultancy
- Development and drafting of SOPs
- Optimisation of quality management systems
- Regulatory support for clinical trial applications
- Support for clients with stored products and day-to-day problem-solving
- Complaint handling
Full-Time Consultancy Services
Our full-time consultants specialise in QA activities such as developing QMS documentation, advising management on regulatory compliance, and helping companies resolve compliance challenges.
We also provide production support and general QA services to companies for which a temporary consultancy solution is the right fit.
Agreements are typically made for a minimum of one month on a full-time basis and billed hourly. Our consultants can work remotely, on-site, or in a hybrid model that suits your preferences.
Areas of expertise:
- Quality Assurance (QA)
- Regulatory Affairs (RA)
- Production Support
- Clinical Affairs
- Qualified Person services (approved QP consultants)
- Regulatory support for clinical trial applications
- Responsible Person services under GDP (approved RP consultants)