Management Team Contact Us

DDIC is headed by Dr. Raimar DDIC welcomes R&D partnerships for

Loebenberg. With over 20 years of Nutraceutical / Natural Health product
experience, he is a recognized expert development, quality control and
in the field and has affiliations to regulatory affairs.
organizations such as:

- American Association of To know more about services that

DDIC can offer please contact:
Drug Development and
Pharmaceutical Scientists (AAPS)
- United States Pharmacopoeia (USP) Innovation Centre
- Health Canada Dr. Raimar Loebenberg
A Premier Centre for
The team members have expertise in Director, DDIC Pharmaceutical Research and
Formulation development, Regulatory Associate Professor Innovation
Affairs and Technology transfer. Faculty of Pharmacy and
Pharmaceutical Sciences
To know more about the management 1123A Dentistry/Pharmacy Centre
team please visit - www.ddic.ca University of Alberta

Edmonton, Alberta - T6G 2N8

Phone: (780) 492 1255

Email: raimar@ualberta.ca
info@ddic.ca
website: www.ddic.ca
Natural Health
Products
Program
 Formulation Development
DDIC is a Health Canada licensed facility for
the manufacturing and development of
Natural Health Products (NHPs). Our team of
experts can provide solutions for your
product development needs for:
ü
Prototype Development
ü
Proof of Concept Studies
ü
Clinical Trial Material Development
üDosage Form Development
Novel
DDIC is equipped with state-of-art
equipments for dosage forms such as:
Oral: Tablets, Capsules, Powders
ú Global linkages
Topical:
ú Ointments, Creams, Lotions,
Emulsions, Suppositories and
Microemulsions
Sterile Dosage Forms
ú
Track record of success
Our clients include the leading NHP
companies in Alberta and Canada.
Analytical Development Regulatory Affairs
DDIC has proven expertise in Quality control DDIC can provide solutions for your
and performance testing of dosage forms. regulatory requirements such as:
Areas of expertise include:
ü
Site License Applications
Dissolution Method Development
ü ü
Product License Applications
Disintegration Testing
ü ü
Quality and Compliance
Analytical Method Development
ü ü
On-site and off-site training in
Stability studies
ü GMP, GLP
Accelerated compatibility studies
ü
using Thermal/ Bioactivity Monitor Proven expertise
Novel dosage form characterization
ü
using Franz Cells and Flow Through ?A GMP compliant Health Canada
Cells approved facility.
?
Successfully filed for product licenses for
various products.
?
Linkages with global organizations such as ?
Trained Health Canada scientists and
inspectors in issues related to Quality
United States Pharmacopoeia and
American Association of Pharmaceutical and Compliance.
Scientists (AAPS).
?
Team members with work experience in
?Enables seamless transition of molecules
from lab to clinic and beyond through major pharmaceutical companies
linkages with NACTRC, ARC ToxTest, Cross
Cancer Institute.
visit us at www.ddic.ca