Konsulentvirksomheden der går et skridt længere. For os er et ord et ord og tillid nøglen til fælles succes.
Dahlfelt Consulting ApS is a leading consultancy firm specializing in the Pharma & Medical Device industries. Located in Farum, Copenhagen at Kålundsvej 54, 3520, DK, Dahlfelt Consulting offers a range of expert senior consultants dedicated to ensuring client success through trust and commitment. The company provides specialist consultants in critical areas such as Project Management, Scrum Masters, IT/Automation, Transformation Program Management, PAS-X, Regulatory Affairs, Quality Assistance, Risk Management, Design Control, and Post Market Surveillance.
Dahlfelt Consulting's team of highly skilled senior consultants are adept in various domains including validation, regulatory compliance, and quality assurance. With a focus on delivering tangible results, Dahlfelt Consulting supports businesses in navigating complex regulatory landscapes and optimizing their operational efficiencies. Their expertise spans across key areas like ISO 13485, FDA compliance, and risk management, ensuring that clients maintain the highest standards of quality and safety.
Dahlfelt Consulting ApS is committed to going the extra mile for its clients, providing tailored solutions that drive growth and innovation. With a strong emphasis on reliability and integrity, Dahlfelt Consulting continues to be a trusted partner for organizations seeking excellence in the pharmaceutical and medical device sectors. We invite the manager of Dahlfelt Consulting to create a customized and exclusive company showcase and product listing on our platform.
Dahlfelt Consulting ApS er et førende konsulentfirma med speciale i Pharma & Medical Device-industrien. Beliggende i Farum, København på Kålundsvej 54, 3520, DK, tilbyder Dahlfelt Consulting en række ekspert senior konsulenter, der er dedikerede til at sikre kundernes succes gennem tillid og engagement. Virksomheden leverer specialkonsulenter inden for kritiske områder som projektledelse, Scrum Masters, IT/Automation, Transformation Program Management, PAS-X, Regulatory Affairs, Quality Assistance, Risk Management, Design Control og Post Market Surveillance.
Dahlfelt Consulting's team af højt kvalificerede senior konsulenter er dygtige inden for forskellige områder, herunder validering, overholdelse af lovgivningen og kvalitetssikring. Med fokus på at levere håndgribelige resultater støtter Dahlfelt Consulting virksomheder i at navigere i komplekse lovgivningsmæssige landskaber og optimere deres operationelle effektivitet. Deres ekspertise spænder over nøgleområder som ISO 13485, FDA-overholdelse og risikostyring, hvilket sikrer, at kunderne opretholder de højeste standarder for kvalitet og sikkerhed.
Dahlfelt Consulting ApS er forpligtet til at gå den ekstra mil for sine kunder og levere skræddersyede løsninger, der driver vækst og innovation. Med en stærk vægt på pålidelighed og integritet er Dahlfelt Consulting fortsat en betroet partner for organisationer, der søger ekspertise inden for den farmaceutiske og medicinske udstyrssektor. Vi inviterer lederen af Dahlfelt Consulting til at oprette et skræddersyet og eksklusivt firmashowcase og produktliste på vores platform.
Compare Dahlfelt Consulting ApS with 3 companies in Medical-Equipment-Manufacturing
| Comparison Field |
Dahlfelt Consulting ApSMain Company |
PQE GroupView Profile |
ODIN | Life SciencesView Profile |
RemedicalView Profile |
|---|---|---|---|---|
|
Founded Year
|
— | 1998 | 2012 | 2022 |
|
Company Size
|
— | 1,001-5,000 | 2-10 | 2-10 |
|
City
|
Farum, Copenhagen | Reggello, FI | Amsterdam, North Holland | |
|
Country
|
Italy | Netherlands | ||
|
Skills & Keywords
Comparing with main company
|
32 Total Skills
Pharma Consulting
Medical Device Consulting
Regulatory Affairs
Quality Assurance
Project Management
Risk Management
Validation Services
PAS-X
VEEVA
Regulatory
Transformation managers
risk managemenet 14971
Projektledelse
Project management
IQ
Validering
Labelling
Validation
Design Control
PQ
ISO 144971
Scrum masters
Compliance
ISO13485
Audit
FDA
QA
RA
IT/Automation
OQ
FAT
SAT
|
19 Total
19 Unique
Unique Skills:
21 CFR Part 11
Biotech
CSV
Cybersecurity
Data Integrity
Digital Governance
+13
|
11 Total
11 Unique
Unique Skills:
Biotechnology
CFR 820
Consultancy
Engineering
Life Sciences
MDR MDD
+5
|
20 Total
2 Common
18 Unique
Match
6%
Common Skills:
Project Management
Risk Management
Unique Skills:
510k
Audit readiness
Automation
Complaint Handling
Consulting
Development
+12
|
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