What benefits does GMP Certification offer?

• GMP consulting services in Jordan will assist in increasing the value of your brand to the point where your sales graph begins to improve.
•  GMP Consulting in Amman can assist you in obtaining orders from the public and government sectors.
•  GMP consulting in Irbid may assist you in reducing unnecessary marketing costs, and increasing gross margin and profit.
•  GMP consultation in Zarqa may help your process become more effective.

How Can One Get GMP Certified In Jordan?

In terms of your certification needs, we are one of the one-stop solution providers. We are a reputable consulting firm that is known all over the globe. We guarantee that your certification requirements have been fully satisfied at a fair price.

 We put a greater emphasis on assisting our clients in getting the most out of the certification and the standard. During the external audit, our expert will assist you in providing proof of the management system that has been put in place to meet the standard requirement. Regardless of business size or annual revenue, it is always clear that with Factocert, GMP Certification cost in Jordan is consistently low and affordable for all of our clients.

A successful manufacturing process may be implemented with the support of GMP standards, which are a set of principles that guarantee quality is ingrained throughout the business and the procedures involved. GMP regulations are typically forgiving, and each nation has its laws that must adhere to its own GMP principles and regulations. However, practically all rules are drawn from the fundamental idea and principles that are:

• Quality Control:

The goal of quality management is to guarantee that produced goods are suitable for their intended use, conform to specifications, and do not endanger customers via insufficient safety, quality, or effectiveness controls. Quality assurance, excellent manufacturing processes, quality control, and quality risk management should be fully and accurately executed to meet this quality aim.

• Quality Management:

The goal of the quality assurance system is to make sure that produced goods are conceived and designed in a manner that complies with GMP standards.

• Guidelines for Good Manufacturing Practice:

Good manufacturing practice is concerned with production and quality control as a component of quality assurance. It seeks to lessen the production-related hazards that are unavoidable. The following are its fundamental needs as stated by WHO’s Good Manufacturing Practices for Pharmaceuticals:

1. All manufacturing procedures are precisely specified, routinely examined in light of experience, and shown to be capable of producing consistently high-quality pharmaceuticals that adhere to their specifications and/or marketing permission.
2.  Validation of crucial manufacturing process stages and substantial process modifications.
3.  All GMP-related facilities, such as:

•  Employees who are suitably qualified and trained;
•  Adequate Premises;
• Appropriate Tools and Services; 
• Right supplies, Packaging, and Labelling
• Authorized Practices and Guidelines;

1. Procedures Written in an instructive format using straightforward language that is directly pertinent to the facilities offered, instructions and procedures;
2.  Operators get the proper training to follow protocols;
3.  During production, records are kept manually or with the use of recording devices to show that all the processes outlined in the procedures and instructions were followed and that the product’s quantity and quality were as anticipated. Any notable differences are thoroughly noted and looked into;
4.  Manufacturing and distribution records that allow for the whole history of a batch to be tracked are kept in a clear and understandable format;
5.  The items’ quality is less at risk due to distribution (wholesaling);
6. There is a procedure in place to stop the sale or supply of any batch of a product;
7. Product complaints are investigated, the sources of quality flaws are looked into, and suitable action is made to address the faulty items and avoid recurrence.

• Quality Assurance:

Good Manufacturing Practice has a component called quality control that emphasizes sampling, specification, and testing. To make sure that goods pass the necessary tests before being launched for sale or supply, it examines the setup, documentation, and release processes.

• Effective Risk Management:

Assessment of risks that may have an impact on product quality is done systematically via the process of quality risk management. Its guiding principles include that good risk management should make sure of the following:

1.  The assessment of the quality risk is based on scientific expertise, and process expertise, and, ultimately, connects to the protection of the patient and users;
2.  The effort, formality, and paperwork put into the quality risk management process correspond to the risk’s magnitude. 

• Cleanliness and Hygiene:

In every step of the production process, sanitation and hygiene are essential. It includes everything that might potentially contaminate a product, including workers, the environment, tools, containers, and manufacturing supplies. A thorough sanitation and hygiene program should be used to identify and eradicate any possible sources of infection.

• Structure and Surrounding Properties:

As a concept, the premises should be positioned in an environment that is suited for its activities and one that is free from hazards of contamination of materials and products. Additionally, the location should be simple to keep clean and maintain and should be built to reduce operational mistakes.

• Equipment:

Similar to the premises, equipment should be positioned, maintained, and designed to work for its intended purpose. It should also be cleaned and preserved following protocols. It should be removed or marked as faulty if there is a flaw or problem.

• Raw Materials:

All production-related materials must be kept appropriately following the guidelines established by the manufacturers. To guarantee that all incoming materials are accurate and of good quality, a suitable stock management system should be put in place.

• Personnel:

The individuals carrying out GMP compliance are crucial to its success. All employees must be trained and competent to do their jobs for this reason. They should be educated on the GMP principles and given ongoing training, and other resources suited to their requirements. Compliant supervisors should be explicit about each employee’s job descriptions to prevent misunderstandings and lower the possibility of problems like overlapping roles.

• Qualification and Attestation:

Validate if processes and procedures can consistently generate high-quality goods by evaluating whether systems, facilities, and equipment are suitable for and ready for the application for which they are intended. Verification of crucial production procedures is necessary to guarantee that high standards of product quality are consistently met. 

• Complaints:

GMP includes handling complaints, thus every manufacturing company should have a GMP complaint procedure that is properly thought out. Ideal complaint management should have a prepared answer to cover all eventualities.

• Record-keeping and Documentation:

The quality assurance system must include effective documentation and record keeping to comply with GMP regulations. Managers and supervisors may maintain track of the historical record of production methods and corrective actions taken with the use of accurate recordkeeping. The following are the standards for documentation generally:

1.  Care must be taken in the design, preparation, review, and distribution of documents.
2.  Written materials should be readable and clear.
3.  Appropriate and authorized employees must approve, sign, and date documents.
4.  The substance of documents, such as their title, nature, and purpose, must be clear.
5.  Documents need to be updated and checked often.
6.  Documents cannot be written by hand.
7.  Any changes to a document or record must be initialled, signed, and dated. Recording the correction’s justification is also necessary (where appropriate).
8.  Keep a record of every step you perform throughout traceable processes like product manufacture and control.

• Examinations and Quality Checks:

Inspections should be carried out often to check on the application and observance of GMP. Record the areas that need more effort and provide remedial actions for ongoing progress. 

Quality audits are performed to evaluate the manufacturing company’s quality systems. Companies may follow GMP regulations established by regulatory agencies with the use of GMP audit checklists. You may find non-compliant processes and act right once to address areas for improvement by carrying out site visual walkthroughs and conducting manufacturer reviews.

How to Comply With the Guidelines of the GMP Standard?

GMP standards and guidelines include a variety of topics that might affect a product’s safety and quality. The firm benefits from adhering to GMP or cGMP standards by increasing the quality of its goods, improving customer satisfaction, increasing revenues, and realizing a lucrative return on investment.

Assessing an organization’s compliance with manufacturing methods and requirements includes doing GMP audits. Regular inspections may reduce the possibility of adulteration and misbrand. The following systems, among others, benefit from an overall improvement in performance brought about by a GMP audit:

1. Facilities and a building
2.  Material Control
3.  Quality assurance procedures
4.  Manufacturing
5.  Identification labels and packaging
6.  Quality control procedures
7.  GMP and personnel training
8.  Purchasing
9.  Customer support

GMP, or good manufacturing practices, guarantee that items are manufactured in a manner that satisfies quality requirements while also controlling quantity.

 GMP takes into account several variables, including cleanliness and environmental conditions. Any faults or abnormalities may be found sooner via this method than they would be after the finished product has been evaluated or is on the market. Ensuring that your goods follow GMP will result in high-quality, safe-for-use or consumption finished products, which will improve customer satisfaction and generate more income.

What criteria must a company meet to be certified under GMP in Jordan?

Once a manufacturer has GMP certification in Jordan, it is its primary obligation to adhere to all the guidelines outlined in the standard to make goods that are entirely safe and sanitary. Typical GMP certification criteria in Jordan include the following:

1. The production process must be preserved in writing, and records must be carefully maintained.
2.  The production space should be kept as clean as possible.
3.  All forms of impurities should be kept out of the production area, and the process should start in a controlled, sanitary atmosphere.
4.  Any changes to the production process must be confirmed right away to stop the development of any form of fault or defect.
5.  Written records of each staff member’s training and experience should be kept.
6.  To ensure a smooth and effective work environment within the production unit, a grievance box must be kept on the company’s property where employee complaints may be filed and promptly resolved.
7.  To maintain the highest degree of cleanliness in the workplace, employees and staff must get the appropriate training.
8.  Employees in management information system departments need sufficient training to keep accurate written records.

A company’s ability to increase client trust that the product they are purchasing is entirely sanitary and devoid of any form of pollutants is aided by receiving GMP certification in Jordan. This immediately aids manufacturers in increasing profits. For more information, you can reach our specialist group from our website:www.factocert.com or get in touch with our team by writing to us at contact@factocert.com and get the answer to all your inquiries.

Why choose Factocert for GMP Certification in Jordan?

Factocert can assist you if you want to learn more about the GMP certification process in Jordan. Our specialists will assist you in obtaining the finest GMP Certification in Jordan at reasonable costs, as well as a certification procedure that runs smoothly.

For more information Visit: GMP Certification in Jordan