PharmEng Announces Opening of Denver Colorado Office
April 20, 2016
PharmEng Technology Inc. is pleased to announce the official opening of our Denver office which will support the biotech, pharmaceutical, and medical device companies in the Rocky Mountain Region, USA. The Denver location provides cost-effective and convenient access for PharmEng to serve Colorado, Nebraska, Utah, Wyoming, Montana, Arizona and the surrounding areas. The Denver office compliments our existing offices in Atlanta and Boston.
"Our cGMP consulting services has grown significantly in the USA and we are committed to expand our scope of services and geographical locations to better serve our customers" explains Alan Kwong, CEO of PharmEng Technology Inc.
About PharmEng Technology Inc.
PharmEng Technology Inc. is a full-service cGMP consulting company that serves the biotech, pharmaceutical and the life science industries in North America and internationally. Our cGMP compliant consulting services include project management, engineering, commissioning, validation, quality assurance and regulatory affairs.
PharmEng Technology and Horizon, Pharmaceutial Consultants, Announce Partnership
Dec. 15, 2014
PharmEng Technology and Horizon (HWT Engineering Ltd.) today jointly announced that they will enter into a collaborative agreement to provide a range of consultancy services to the Pharmaceutical industry worldwide. This arrangement will see both PharmEng and Horizon take advantage of their excellent positioning in North America and Europe respectively by enabling this partnership the ability to efficiently and effectively deliver a suite of services to their clients requiring expertise in Pharmaceutical Engineering, Quality and Validation.
PharmEng Technology CEO, Alan Kwong, said at today’s announcement, ‘I am excited by this partnership which provides a global platform with combined resources to ensure first class service to our worldwide clients.’
PharmEng Technology is a global Pharmaceutical compliance consulting firm with projects around the world providing quality services to the manufacturers of health care products for over 15 years. PharmEng Technology is a cGMP compliant leader in commissioning and qualification, validation, quality systems, regulatory affairs, engineering, auditing, process development, technology transfer, serialization and training.
Horizon is an award winning global specialist engineering consultancy that provides solutions to manufacturing organisations primarily in the areas of Medical Device, Pharmaceutical and Bio- Technology. Horizon’s offerings are across 3 key operations, Resourcing, Engineering & Development and New Product Development. With a diverse client base across Europe and the US, Horizon provides engineering services to over 50% of the top global life science companies.
Aiden Corcoran CEO of Horizon, said of the Partnership, ‘I’m really excited to be partnering with PharmEng. Together we can offer greater depth in terms of specialist skill supply to both the European and North American regions.’
cGMP Compliance Audit: 5 Questions You Should Ask Yourself
Jan 5, 2015
PharmEng Technology published an article written by one of their Senior Consultants, Dr. Peter Chan. Dr. Chan is a senior quality compliance specialist with 16 years of diversified experience in project management, quality assurance, quality control, validation, regulatory compliance and pharmaceutical manufacturing.
PharmEng Technology Is Your Leading Serialization Expert
May 5, 2014
PharmEng Technology has been awarded a significant multi-site serialization project with a multinational Biopharmaceutical company. Our subject matter experts can ensure that you are compliant with the new serialization requirements that will take effect in 2015. Please contact us at 416-385-3922 ext 103 if you are in need of support.
We Understand The East And The West - Business Elite Canada
PharmEng Technology is so excited to have been part of the April 2014 issue of the Business Elite Canada magazine. The author, Mudeeha Yousaf, interviewed Alan Kwong, CEO of PharmEng Technology, to determine what sets us apart from other companies in our industry and how we have succeeded over the years. Please find out 6 pages spread titled "We Understand The East And The West" here.
PharmEng Receives Recertification For ISO 9001:2008
April 14, 2014
PharmEng Technology has been recertified with the International Organization for Standardization. This certification ensures that we operate a quality management system which complies with the requirements of ISO 9001:2008. ISO helps to harmonize technical specifications of products and services making our operations as efficient as possible, which increases productivity and allows us to provide the most cost effective service to our clients.
Pharmaceutical Regulatory Summit Asia in Beijing, China
March 25-28, 2014
PharmEng Technology will be attending the Pharmaceutical Regulatory Summit Asia in Beijing, China for a workshop – Preparing and Submitting Dossiers for Generic Drug Approval.Please Click here for more information on the Pharmaceutical Regulatory Summit Asia.
Kenny Peng Speaks at the Hong Kong Pharmacy Conference
March 15-16, 2014
Kenny Peng, Director from PharmEng Technology, will be speaking at the Hong Kong Pharmacy Conference 2014.
Date: March 16, 2014
Time: 11:00am – 11:40am
Topic: Design of a PICS/S GMP Biological Facility – an experience from Taiwan
Please click here for the agenda.
PharmEng Technology Sends Consultants to Shanghai, China to Assist a Major Pharmaceutical Company
February 28, 2014
PharmEng has been engaged as Director of Commissioning, Qualification, and Validation for a new aseptic biopharmaceutical facility in Hebei, China. The project, backed by the Client's US parent company, is conducted in collaboration with a local CQV team in Shanghai, China.
PharmEng Technology Exhibits INTERPHEX 2014 in New York City – March 18-20, 2014 BOOTH #2457
February 24, 2014
Please visit us at INTERPHEX 2014 which will be held at the Javits Center in New York City March 18-20, 2014. Click here to register as our guest and receive FREE exhibit hall admission.
For more information on INTERPHEX click here.
PharmEng Technology Provides QA Support to a Major Medical Marijuana Facility
February 21, 2014
PharmEng Technology has been engaged by a large Medical Marijuana Manufacturer to develop all their quality systems. We will be working with them to ensure that they are in compliance with federal regulators in order to obtain their site licence.
PharmEng Technology starts the new year of 2014 with a big bang!
February 3, 2014
PharmEng begins 2014 with a big bang as we have been engaged by a multi-national pharmaceutical company for a significant decommissioning project.
PharmEng Technology contributes to ISPE magazine Pharmaceutical Engineering (July/August 2013)
Congratulations to Kenny Peng, Director of Aisa for PharmEng Technology, on the publication of his article, “Good Manufacturing Practices for Halal Pharmaceuticals,” in the July/August issue of Pharmaceutical Engineering magazine!
PharmEng Technology is now certified to ISO9001:2008!!!
June 10, 2013
ISO 9001 is an international quality standard developed by the International Organization for Standardization (ISO), a worldwide federation of national standards bodies representing some 130 countries. It provides a structured yet flexible framework for a customer focused business management system that will drive business performance improvement.
April 16, 2013
NMSDC’s rigorous certification process is considered the gold standard for certifying minority-owned businesses by corporate America. The NMSDC Affiliate Regional Councils located throughout the country are responsible for certifying businesses owned by Asian, Black, Hispanic and Native American business owners using guidelines established by the National Minority Supplier Development Council.
April 16, 2013
CAMSC corporate members are investing in an inclusive supply chain for a variety of reasons, such as the opportunity to access newer innovative suppliers, as well as the opportunity to create wealth, employment, and build brand loyalty with aboriginal and minority communities.
April 10, 2013
The RAPS Feature article on Singapore GDPMDS compared to ISO 13485 is shown up on the Regulatory Affairs Professionals Society website for May edition. It is co-authored by Kenny Peng, Director of Asia for PharmEng Technology.
You can read it up here.
April 3, 2013
Kenny Peng from PharmEng Technology will be featured as a speaker at the ISPE China Annual Meeting 2013. On April 22 at 8:05am-8:30am (Track A), Mr. Peng will be presenting Good Distribution Practices - A Case Study on an International Technology Transfer.
Please click here for more information about ISPE China Annual Meeting.
March 3, 2013
PharmEng Technology will be at the National University of Singapore presenting a training program on Computerized System Validation. The program takes place on March 14-15, 2013 from 9am-5pm. Please follow this link for more information.
PharmEng Technology will be at the National University of Singapore presenting a training program on Fundamentals of Regulatory Affairs. The program takes place on March 20-21, 2013 from 9am-5pm. Please follow this link for more information.
More courses under NUSAGE-PHARMENG Pharmaceutical and Technology Training Program are coming:
22-23 Aug. 2013 Analytical Method Validation
18-19 Sept. 2013 Equipment Qualification for Pharmaceutical Facility
24-25 Oct. 2013 Effective Quality Assurance-Audits, Annual Review, Events Handling and CAPA
14-15 Nov. 2013 Distribution, Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices Internationally
10-11 Dec. 2013 Stability Studies for Pharmaceutical Products (API and Finished Products)
February 22, 2013
February 18, 2013
January 29, 2013