Herlev Pharma Service ApS provides consulting and GMP Storage services for small biotech and pharma companies.
Herlev Pharma Service ApS specializes in providing comprehensive consulting and GMP storage services to small biotech and pharmaceutical companies. Located at Herlev Hovedgade 195, 3. tv, Herlev, DK-2730, DK, Herlev Pharma Service ApS is dedicated to supporting the pharmaceutical industry with top-tier logistics and storage solutions.
With a focus on handling, distribution, import/export, warehousing, and release of drug products, APIs, IMPs, and finished medical products, Herlev Pharma Service ApS ensures that all client needs are met with the highest standards of quality and compliance. The company's expertise in GMP and GDP allows it to offer unparalleled service in the pharmaceutical sector.
Herlev Pharma Service ApS is committed to facilitating the success of its clients through reliable and efficient services. We look forward to sharing more detailed information about how Herlev Pharma Service ApS can meet your specific needs, which will be completed soon with the support of the company’s management. Company manager, we invite you to create a customized and exclusive company showcase and product listing on our platform.
Compare Herlev Pharma Service Aps with 3 companies in Business-Consulting-and-Services
| Comparison Field |
Herlev Pharma Service ApsMain Company |
QualifyzeView Profile |
HEISView Profile |
Nimuee Pharmaceutica...View Profile |
|---|---|---|---|---|
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Founded Year
|
— | 2019 | 2011 | 2016 |
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Company Size
|
— | 51-200 | 2-10 | 11-50 |
|
City
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Frankfurt, Hesse | Freiburg im Breisgau, Baden-Württemberg | Ahmedabad, Gujarat | |
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Country
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Germany | Germany | India | |
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Skills & Keywords
Comparing with main company
|
14 Total Skills
Pharmaceutical Consulting
GMP Storage
Biotech Services
Drug Product Handling
API Distribution
IMP Logistics
Medical Product Warehousing
GMP
Logistik
Medical Device
IMP
GDP
QP Release
Audits
|
12 Total
12 Unique
Unique Skills:
Audit reports
Auditors
Compliance
Digitalization
GxP
ISO90001
+6
|
18 Total
18 Unique
Unique Skills:
Analysis
Consultation
Development
DHF
EU MDR 2017
FDA 21 CFR 820
+12
|
9 Total
9 Unique
Unique Skills:
Certification
Computer System Validation
Consultation
Cosmetics
Data Integrity
Export
+3
|
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