DI Regulatory Consultants Email Formats
Pharmaceutical Manufacturing • 
Cape Town, Western Cape, South Africa • 21-50 Employees
DI Regulatory Consultants Email Formats
DI Regulatory Consultants uses 3 email formats. The most common is {first name}.{last name} (e.g., john.doe@diconsultants.co.za), used 57.9% of the time.
| Format | Example | Percentage |
|---|---|---|
{first name}.{last name} | john.doe@diconsultants.co.za | 57.9% |
{first initial}.{last name} | j.doe@diconsultants.co.za | 42.1% |
Key Contacts at DI Regulatory Consultants
Emtia Perold
Managing Director
Rudi Oliver
Director
Charmaine Van Eeden
Director
Heleen Oliver
Operational Director
Company overview
| Headquarters | 10 Church Street, Durbanville, Cape Town, Western Province 7551, ZA |
| Phone number | +27182974072 |
| Website | |
| NAICS | 3254 |
| SIC | 283 |
| Keywords | Pharmacovigilance, Quality Management Systems, Biosimilars, Cosmetics, Due Diligence, Medical Devices, Licencing, Veterinary Medicines, Ectd, Regulatory Management, Complementary Medicines, Pharmaceutical Regulatory, Protocol Management, Gxp Audits, Pharmaceutical Labeling, Biological Medicines, New Chemical Entities, Act 101 Medicine Registrations, Africa Regulatory Submissions, Common Technical Dossiers (Ctd), Dalrrd Applications, Document Management System (Docubridge), Dossier Lifecycle Management |
| Founded | 1993 |
| Employees | 21-50 |
| Socials |
About DI Regulatory Consultants
DI Medicine Regulatory Consultants has been serving the pharmaceutical industry for over 30 years with comprehensive expertise and understanding of the current and ever changing regulatory environment. We offer a complete range of medicine regulatory consulting services throughout South Africa and Africa. Our services include, but are not limited to the regulatory consulting for human medicines, veterinary medicines, medical devices, complementary medicines and cosmetics. We also provide regulatory consulting services for other African countries. We provide assistance with Licence applications and the relevant Quality Management Systems thereof, including Standard Operating Procedures (SOPs), Site Master Files (SMFs), Quality Manuals (QMs) and Pharmacovigilance Management Systems. In addition we assist with GxP preparation by providing world class auditing services based on current Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and Good Wholesale/Warehouse Practice (GWP) as required.
Employees by Management Level
Total employees: 21-50
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Employees by Department
DI Regulatory Consultants has 15 employees across 4 departments.
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Funding Data
DI Regulatory Consultants has never raised funding before.
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