DI Regulatory Consultants
Pharmaceutical-Manufacturing
Website
Company Tagline
Prompt - Professional - Cost-effective
Industry Category
Business Keywords
Company Description
DI Regulatory Consultants has been a steadfast partner to the pharmaceutical industry for over three decades, offering unparalleled expertise in navigating the dynamic regulatory landscape. With a commitment to prompt, professional, and cost-effective solutions, DI Regulatory Consultants delivers comprehensive medicine regulatory consulting services throughout South Africa and Africa.
Located at the primary address of 10 Church Street, Durbanville, Cape Town, Western Province 7551, ZA, and with additional offices at 8 Venter Street, Potchefstroom, North West Province 2531, ZA, and 16 Pieter Street, Manhattan Office Park, Unit 2, City of Tshwane, Gauteng 0157, ZA, DI Regulatory Consultants provides expert assistance with license applications, Quality Management Systems (including SOPs, SMFs, and QMs), and Pharmacovigilance Management Systems. The company also excels in GxP preparation, delivering world-class auditing services based on current Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Wholesale/Warehouse Practice (GWP).
DI Regulatory Consultants specializes in regulatory consulting for human medicines, veterinary medicines, medical devices, complementary medicines, and cosmetics. Their proficiency extends to biosimilars, Act 101 medicine registrations, pharmaceutical labeling, document management systems (DocuBridge), eCTD, DALRRD applications, dossier lifecycle management, and Africa regulatory submissions. DI Regulatory Consultants remains dedicated to supporting the pharmaceutical industry's growth and compliance.
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DI Regulatory Consultants is sedert meer as drie dekades 'n standvastige vennoot vir die farmaseutiese bedryf, en bied ongeëwenaarde kundigheid in die navigasie van die dinamiese regulatoriese landskap. Met 'n verbintenis tot vinnige, professionele en koste-effektiewe oplossings, lewer DI Regulatory Consultants omvattende medisyne regulatoriese konsultasiedienste in Suid-Afrika en Afrika.
Geleë by die primêre adres van 10 Church Street, Durbanville, Kaapstad, Wes-Kaap 7551, ZA, en met addisionele kantore by 8 Venterstraat, Potchefstroom, Noordwes Provinsie 2531, ZA, en 16 Pieterstraat, Manhattan Office Park, Eenheid 2, Stad van Tshwane, Gauteng 0157, ZA, verskaf DI Regulatory Consultants deskundige bystand met lisensie aansoeke, Kwaliteit Bestuurstelsels (insluitend SOPs, SMFs en KMs), en Farmakovigilansie Bestuurstelsels. Die maatskappy blink ook uit in GxP-voorbereiding, en lewer ouditdienste van wêreldgehalte gebaseer op huidige Goeie Vervaardigingspraktyk (GMP), Goeie Laboratoriumpraktyk (GLP) en Goeie Groothandel/Pakhuispraktyk (GWP).
DI Regulatory Consultants spesialiseer in regulatoriese konsultasie vir menslike medisyne, veeartsenykundige medisyne, mediese toestelle, komplementêre medisyne en skoonheidsmiddels. Hul bekwaamheid strek tot biosimilêre middels, Wet 101 medisyne registrasies, farmaseutiese etikettering, dokumentbestuurstelsels (DocuBridge), eCTD, DALRRD aansoeke, dossier lewensiklusbestuur, en Afrika regulatoriese voorleggings. DI Regulatory Consultants bly toegewyd om die farmaseutiese bedryf se groei en nakoming te ondersteun.
Ons nooi die bestuurder van DI Regulatory Consultants uit om 'n pasgemaakte en eksklusiewe maatskappyvertoning en produkaanbieding op ons platform te skep.
Key Personnel / Employees
Compare Companies Side by Side
Compare DI Regulatory Consultants with 3 companies in Pharmaceutical-Manufacturing
| Comparison Field |
DI Regulatory ConsultantsMain Company |
Bizaffairs, Unipesso...View Profile |
Bionok Healthcare -...View Profile |
Pharmakon Consultant...View Profile |
|---|---|---|---|---|
|
Founded Year
|
— | 2008 | 2012 | 2020 |
|
Company Size
|
— | 2-10 | 11-50 | 1 employee |
|
City
|
Cape Town, Western Province | Madrid, Madrid | Montreal, Quebec | |
|
Country
|
South Africa | Spain | Canada | |
|
Skills & Keywords
Comparing with main company
|
28 Total Skills
Pharmaceutical Regulatory Consulting
GxP Audits
Medicine Regulatory Services
Quality Management Systems
Pharmacovigilance
GMP
Regulatory Submissions
Cosmetics
Biosimilars
Veterinary Medicines
Licencing
Act 101 Medicine Registrations
Pharmaceutical Labeling
Document Management System (DocuBridge)
eCTD
DALRRD Applications
Pharmaceutical Regulatory
Dossier Lifecycle Management
Complementary Medicines
Common Technical Dossiers (CTD)
Biological Medicines
Medical Devices
New Chemical Entities
Africa Regulatory Submissions
Artwork/Advertisements Translations & Proofreading
Protocol Management
Due Diligence
Regulatory Management
|
8 Total
8 Unique
Unique Skills:
Biocides
CE Marking
Clinical Trials/Studies
Cosmetovigilance
Drug Products
Food Supplements
+2
|
11 Total
11 Unique
Unique Skills:
Biocides
Consulting
Detergency
EU Compliance
Food Supplements
Ingredients
+5
|
19 Total
19 Unique
Unique Skills:
APAC
Audit Readiness / Enforcement
AUS/NZ
Baseline Asessments
CAPA Management/Effectiveness Monitoring
EMA & non-EU
+13
|
4
Total Companies2008
Oldest Founded3
Countries62
Unique SkillsSimilar Companies
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Alternative Company Names
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