Technical Writing Clients Click a company logo for a description of some of the tasks performed.
Wrote/revised over 70 production procedures (SOPs) and work instructions for this manufacturer of medicated confectioneries.
Guided client through review and approval process to meet tight timeline.
The Apotex Pharmaceutical Group of Companies develops and manufactures generic pharmaceuticals, researches, develops, manufactures and distributes fine chemicals, non-prescription and private label medicines, and disposable plastics for medical use.
Performed technical writing for the Validation Services and Facility departments.
Coordinated technical writing project producing Quality Assurance documents for Innovative Drug Development.
Wrote Site Reference Files for the company's main packaging, warehousing, fabricating and distribution facilities.
Bausch & Lomb's core businesses include soft and rigid gas permeable contact lenses and lens care products, and ophthalmic surgical and pharmaceutical products.
Prepared and revised SOPs for warehouse-related activities.
Biovail Corporation is a specialty pharmaceutical company that applies advanced drug-delivery technologies to improve the clinical effectiveness of medicines. The company's therapeutic areas of focus are central nervous system (CNS) disorders, pain management and cardiovascular disease.
Reviewed and updated site reference file.
Wrote Site Reference File for medical gas operations facility.
Cadbury is a confectionery and beverages company. Today their products include brands such as Cadbury, Schweppes, Halls, Trident, Dr. Pepper, Snapple, Trebor, Dentyne, Bubblicious, and Bassett.
Wrote SOPs and work instructions in preparation for AIB audit (approximately 25 SOPs, 300 forms - work instructions and checklists).
Produced Standard Operating Procedures (SOPs) for Quality Control Laboratories, Facilities Services, Product Services, Order Services, and Order Fulfillment for this manufacturer of pharmaceutical products, whose drugs include those to treat depression, schizophrenia, attention-deficit hyperactivity disorder, diabetes, osteoporosis and many other conditions.
Produced 40 integrated SOPs for the manufacture, packaging and testing of liquid and tablet products at a company who specializes in pharmaceuticals, nutrition, eye-care, and animal health.
Provided guidance on improvements necessary to bring processes up to Canadian and U.S. GMP standards.
Sanofi Pasteur is the country's largest vaccine company with a proud heritage and commitment to public health. They provide important and superior vaccines for the prevention and treatment of infectious diseases, common illnesses and cancers.
Wrote and updated numerous policies and procedures to new company standard for a wide range of departments (QA, QC, production, maintenance, etc.) ensuring compliance with GMPs and cGMPs.
Wrote detailed SOPs for manufacturing and packaging operations for Taro, who manufactures and markets high quality medications, sold by prescription and over-the-counter.
Wrote technical documentation and SOPs for research laboratory for Torcan, who offers chemistry services ranging from preclinical development to commercial manufacturing. They also do contract research, development and manufacture of active pharmaceutical ingredients, and advanced intermediates.
Since 1994 Quality & Compliance Services Inc.
(Q&C®) has provided consultation, auditing,
regulatory services, validation, training,
technical writing, Quality Control Officer
services (including product release), and lab
services to a broad range of clients.
Why Hire Us for
Technical Writing?
By hiring us to complete your technical writing tasks, your staff will be able to focus on regular business. This, combined with our ability to complete the work quickly, means the impact on your bottom line is minimized. Our studies show that your staff saves (on average) 80% of the time it would take them to generate a technical document themselves.
Much of this work can be performed off-site; office space, computers, and support staff, are not required. We communicate regularly with you and transfer documents via e-mail as they are ready for review.
You will retain all documentation at the end of the project. We provide documents in your preferred format that are clear, accurate, and easy to use.
In some instances, we have assisted in
wide-ranging upgrades of corporate quality and
compliance support systems. In others, we have
helped clients respond to specific regulatory
demands under stringent time constraints. In
all cases, our hallmark has been professional,
timely, and efficient delivery of work that was
both accurate and complete.