As an OEM contract manufacturing company headquartered in Singapore, we have operated under the strict regulations of the laws of the Republic of Singapore for over 15 years. All business operations are carried out according to quotations and contracts concluded between us and our clients after relevant negotiations. The subsequent contract manufacturing agreement is an important step in protecting our customers and us so that contract manufacturing work is done from start to finish to the specified product so that the finished product meets our customer’s business needs and is permitted to be marketed in accordance with current regulations.
Before the two parties sign and approve the agreement, pharmaceutical contract manufacturing companies will discuss the details of contract manufacturing accordingly, including contract manufacturing product name, price, packaging specifications, production quantity, delivery lead time, testing requirements, production loss standards , quality and other specifications. Standards, raw material standards, warehousing standards, payment terms, delivery address, breach of agreement terms, etc. After both parties agree on the contract manufacturing details, the contract is signed and approved by both parties, and both parties retain a copy of the original agreement.
In addition to confirming the pharmaceutical contract manufacturing agreement, a non-circumvention, confidentiality and non-disclosure agreement is attached to protect product formulation, price and intellectual property rights related to the product. For customers who have not signed this confidentiality agreement, our company will abide by business ethics and do our best to prevent the disclosure of customer-related information to another party.
As a pharmaceutical contract manufacturing company, we understand the importance of the raw materials that our customers send in as their key assets, so we will handle the materials in our stores in accordance with GMP standards. After the raw materials are rationally used for production, the remaining materials are properly stored in accordance with GMP standards, and the finished products are returned to customers after they leave the factory, with labels clearly indicating the expiration date and storage requirements of the materials. remaining material. For customers who need a solution for short-term storage of surplus material after production is complete, this can be added to the agreement as an additional fee-based service, the material can be retained for the next repeat order of the product or when the surplus material is ready by Our customers collect.
As a Singapore registered GMP certified pharmaceutical contract manufacturing pharmaceutical company, we can include our GMP certificate in the product packaging design according to the client’s request, which will be included in the contract manufacturing agreement. Any reasonable use of our GMP certificate without taking advantage of our brand rights can be specified in the agreement with the client. At the same time, any use of our client’s branding and other relevant information can similarly be included in the agreement, and use is permitted only after our client’s written confirmation.