Company Tagline
Regulatory, Quality Assurance and Clinical Affairs Experts for the medical device and life science industries
Industry Category
Business Keywords
Company Description
LDP Consulting excels in providing comprehensive services in Regulatory, Quality Assurance, and Clinical Affairs for the medical device and life science industries. With years of experience and in-depth knowledge, LDP Consulting supports projects with a wide scope of services tailored to meet specific needs.
LDP Consulting's primary address is Hey Beiyar Street, 44, Tel Aviv, IL. The company is dedicated to offering expert support in navigating the complex landscape of medical device regulations and quality standards. LDP Consulting ensures clients achieve and maintain compliance, facilitating market access and product success.
With a focus on regulatory submissions, clinical trials, and quality management systems, LDP Consulting enhances the commercial development and sales potential of its clients. We invite the manager of LDP Consulting to create a customized and exclusive company showcase and product listing on our platform to further amplify their market presence.
Key Personnel / Employees
Compare Companies Side by Side
Compare LDP Consulting with 3 companies in Medical-Equipment-Manufacturing
| Comparison Field |
LDP ConsultingMain Company |
qualityworks.View Profile |
Fang ConsultingView Profile |
Medpoint, LLCView Profile |
|---|---|---|---|---|
|
Founded Year
|
— | 0 | 1999 | 2002 |
|
Company Size
|
— | 1 employee | 11-50 | 11-50 |
|
City
|
Roseville, MN | Greenville, South Carolina | ||
|
Country
|
United States | United States | ||
|
Skills & Keywords
Comparing with main company
|
15 Total Skills
Medical Device
Regulatory Affairs
Quality Assurance
Clinical Affairs
ISO 13485
MDR Compliance
FDA Submission
MDR 2017/745
FDA submission
MDR submission
Clinical trials
Internal Audits
IVDR 2017/746
IVDR submission
ISO 14155
|
3 Total
3 Unique
Unique Skills:
CE Marking
CFR 21 PART 820
MDSAP
|
15 Total
15 Unique
Unique Skills:
21 CFR
510(k)
CE Mark
Class I
Design Dossier Preparation
FDA
+9
|
9 Total
9 Unique
Unique Skills:
Biotech
ISO13485
ISO17025
ISO9001
Permanent Placement
Pharmaceutical
+3
|
4
Total Companies1999
Oldest Founded1
Countries42
Unique SkillsSimilar Companies
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Alternative Company Names
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