
CDMO Service Provider
Recently, the opening ceremony of Suzhou Olipharma Technology Co., Ltd.'s oligonucleotide drug CDMO platform was successfully held at Phase I of LifeBay, Wuzhong Pharmaceutical Industry Park.
The opening ceremony was hosted by Dr. Wang Yunduan, Vice General Manager of Olipharma. Government leaders attending the event included Gu Hongjian, member of the Working Committee of Wu Zhong Economic Development Zone and Deputy Director of the Management Committee, Li Ji, Director of the Investment Promotion Bureau of Wu Zhong Economic Development Zone, and Tong Tong, Chairman of Wu Zhong Biomedical Industry Development Co., Ltd. Additionally, Sun Linghao, Managing Director of Matrix Partners, Li Jing, Vice President of Clearpine Capital, Zhang Lu, Partner of Yida Capital, along with Zhao Hai, Founder of Olipharma, and representatives from Olipharma's partner companies were present at the opening ceremony.
On-site Speech
Mr. Zhao Hai, founder and general manager of Olipharma, stated in his speech: "As a technical service company dedicated to the nucleic acid drug field, we feel deeply honored to be able to contribute to this industry. With the official opening of Olipharma's oligonucleotide drug CDMO platform, we have reached an important milestone."
Subsequently, General Manager Zhao expressed heartfelt gratitude to the leaders at all levels, investors, teams, and partners for their care and support given to Olipharma.
In the future, Olipharma will steadfastly forge ahead to build a high-standard nucleic acid drug production platform and system in China, better serving nucleic acid innovative drug companies, accelerating the research and development and production of nucleic acid drugs, contributing Chinese strength to the industry's development, and shouldering the mission of "making nucleic acid drugs benefit the world!"

Subsequently, Mr. Gu Hongjian, member of the Party Working Committee and Deputy Director of the Management Committee of Wu Zhong Economic Development Zone in Suzhou, delivered a speech. Director Gu extended his warm congratulations on the opening of Olipharma's oligonucleotide drug CDMO platform.
He pointed out that Wuzhong Economic Development Zone, as the main battleground and primary engine for Wuzhong's economic development, has already attracted over 400 well-known enterprises, including Fortune 500 companies like Corning from the United States and GlaxoSmithKline, to establish operations. It is gradually becoming a highland for biopharmaceutical innovation in the Yangtze River Delta region with comprehensive R&D capabilities and a complete range of pharmaceutical categories.
Mr. Gu Hongjian mentioned that the technical team of Olipharma comes from one of the earliest groups in China to engage in the development of nucleic acid drug production processes and CMC research, with rich experience in project development and product registration. They have successively received honorary titles such as "Suzhou Innovative Small and Medium-sized Enterprise," "Top 100 Future Healthcare Enterprises by VCBeat," "2023 Dongwu Leading Talent in Innovation and Entrepreneurship," and "2023 Gusu Leading Talent in Innovation and Entrepreneurship." The successful establishment of Olipharma in Wuzhong Economic Development Zone will greatly promote the industrial clustering and industry development of the nucleic acid drug sector in Wuzhong District.
He emphasized that Wu Zhong Economic Development Zone's "industry-strong district, innovation-led" development strategy consistently supports the growth of enterprises within the zone, providing optimal services to businesses with dedication and effort, and jointly creating a bright future for Wu Zhong's biopharmaceuticals industry.

Mr. Li Jing, Vice President of Qingsong Capital, delivered a speech on behalf of the investors. He stated that nucleic acid drugs are currently a hot topic and frontier in the pharmaceutical field, possessing tremendous potential and broad application prospects. However, the development of the nucleic acid drug industry requires support from professional teams, capital, government departments, and individuals from all sectors of society. Olipharma, as a professional CDMO company for oligonucleotide drugs, will focus on helping customers address key challenges such as process scale-up and CMC control in small nucleic acid drug manufacturing. Qingsong Capital is an entrepreneurial private equity investment firm specializing in biotechnology and healthcare, with a management team that has deep industry backgrounds and extensive experience in private equity investment. On the occasion of this opening, let us wish Suzhou Olipharma Technology Co., Ltd. continued success and further important contributions to the development of nucleic acid drugs in China.

About Olipharma
Suzhou Olipharma Technology Co., Ltd. is a professional pharmaceutical nucleic acid CDMO company that provides customers with "one-stop" services ranging from nucleic acid drug discovery, laboratory R&D, process and analytical development, CMC services, API production, to drug registration. The technical team of Olipharma comes from one of the earliest teams in China to engage in the development of nucleic acid drug manufacturing processes and CMC research, possessing extensive experience in project development and product registration. Currently, the company has established four industry-leading core technology platforms: solid-phase nucleic acid synthesis, chemical modification and conjugation, process development and analysis, as well as CMC pharmaceutical research. It has also entered into in-depth collaborations with multiple pharmaceutical companies and biotechnology firms both domestically and internationally.
In 2023, the company's 3,000-square-meter GMP-compliant pilot platform officially began offering services, focusing on helping customers address critical challenges such as small nucleic acid drug process scale-up and CMC pharmaceutical research. The company will continue to provide compliant, high-quality, reliable, and efficient services to help customers improve R&D efficiency, accelerate product registration and market entry, and jointly support the entire process of small nucleic acid drugs from preclinical to commercial production.
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