Jakim to Invest Millions in Halal Lab

Oct 23rd, 2008
Katie Schaefer
CT.com_TestTubes

An increasing demand for halal products has spurred the Islamic Development Department (Jakim) to set up a multi-million laboratory to perform sophisticated and advanced tests to determine the halal worthiness of any product, reported The Star online. The laboratory, reportedly estimated to cost around RM21 million will be ready by 2011 and will provide a close collaboration between the department and University Putra Malaysia (UPM), known for its tests, research work and R&D development for halal products.

The facility will be located at the Halal Management Complex at Bandar Einstek, located in Nilai, Negri Sembilan. Jakim director-general Datuk Wan Mohammad Sheikh Abdul Aziz said the laboratory, once in operation, would expedite tests being conducted on products before they could be certified as halal, adding customers' concern has resulted in many companies applying for halal certification from the department.

In 2005, Jakim reportedly received 716 applications for its halal certification while last year, the number of applications received surged to 1,743. Currently, the department has to depend on the Chemistry Department to help carry out tests before it could issue a halal certificate.

As defined by Merriam-Webster, halal refers to a material as being sanctioned by Islamic law, especially as ritually fit for use.

More in Regional
The anti-stress mineral concentrate for sublimated skin
Sponsored
The anti-stress mineral concentrate for sublimated skin
SILAB presents MYOLINE®, a natural relaxing active ingredient and genuine plant "botox-like". MYOLINE® counteracts the deleterious effects of psychological stress on the skin, leaving it younger and more radiant.
Jan 19th, 2024
Xforms is just one digital option available for creating an SPL file with cosmetic product facility registration and product listing information. Two additional electronic options are available.
FDA Debuts Digital SPL Xforms, Paper Forms for Cosmetics Facility, Product Submissions
The FDA has rolled out Structured Product Labeling (SPL) Xforms, a digital tool, and downloadable PDF forms to register cosmetic product facilities and list products, as mandated by MoCRA.
Jan 10th, 2024
“We are excited to welcome Emily back to lead our legal team and guide our industry’s legal and regulatory strategies,” said Tom Myers, PCPC’s president and CEO. “Her diverse and extensive expertise will be instrumental in navigating our industry’s complex legal and regulatory landscape, enhancing our support to member companies.”
The Personal Care Products Council Names VP Legal and Regulatory Affairs and General Counsel
Manoso previously worked as PCPC’s associate general counsel and staff counsel and has served as a trail attorney for the U.S. Department of Justice.
Jan 5th, 2024
Fda Computer Screen Adobe Stock 516632560 Editorial Use Only
FDA Opens Cosmetics Direct Registration Portal for MoCRA
Cosmetics Direct is an FDA Structured Product Labeling authoring tool that, according to the FDA, features user-friendly data entry forms.
Dec 18th, 2023
A responsible person is required to report serious adverse events associated with the use of cosmetic products in the U.S. to FDA within 15 business days.
FDA Releases Update to Ongoing Activities Related to Serious Adverse Event Reporting for MoCRA
A responsible person is required to report serious adverse events associated with the use of cosmetic products in the U.S. to FDA within 15 business days.
Dec 15th, 2023
According to the European Commission's Safety Gate, numerous products, ranging from soaps and fragrances, to body care, shampoo, bath milk and others, have been flagged for the present of the fragrance allergen butylphenyl methylpropional.
Recall Alert: L'Oreal's Mizani, J&J's Clean & Clear, Marcelle's 40+ Cream and Others
Globally, within the past couple of months, numerous cosmetic product recalls have been issued for microbe contamination and fragrance allergens, among other contaminants. Following is a roundup.
Dec 4th, 2023
'I think the biggest game-changer about [MoCRA's] ... requirement for GMPs is how it changes what it means to be adulterated,' Brandi Reinbold, senior manager of global certification for NSF International, said in this sponsored videocast. Register now to watch and learn more. It's free.
[video] GMP Standards to Meet MOCRA and Retailer Mandates of the Future
While the enforcement of MoCRA has been delayed until July 1, 2024, this is no time to rest on our laurels. As this sponsored video from NSF International explains, there's much to do and it will take time. Register now to watch and learn how to prepare.
Nov 27th, 2023
Beginning Dec.1, 2023, domestically produced toothpaste must be notified with the provincial-level drug supervision and administration department in the jurisdiction of the notification applicant before being marketed and sold.
China National Medical Products Administration Updates Toothpaste Regulations
Beginning Dec.1, 2023, domestically produced toothpaste must be notified with the provincial-level drug supervision and administration department in the jurisdiction of the notification applicant before being marketed and sold.
Nov 21st, 2023
The FDA does not intend to enforce the requirements related to cosmetic product facility registration and cosmetic product listing for an additional six months after the December 29, 2023, deadline.
FDA Delays MoCRA Enforcement by 6 Months
The U.S. Food and Drug Administration (FDA) announced it will delay the enforcement of facility registration and product listing requirements under MoCRA for six months after the Dec. 29, 2023, deadline to give the industry "sufficient time" to submit.
Nov 8th, 2023
While the concerns expressed over these materials are not specific to cosmetics, and only two are currently listed as cosmetic ingredients, it is worth noting the potential safety issues of these materials as well as the likelihood of the bans initiated in California to spread nationwide.
California Bans 4 Food Additives, FDA Proposes Same for BVO Emulsifier
On Oct. 7, 2023, the State of California banned four food and beverage additives reportedly linked to health issues: potassium bromate, propyl paraben, Red Dye No. 3 and brominated vegetable oil (BVO). The FDA may follow suit with BVO.
Nov 7th, 2023
October was the deadline but it came and went without a MOCRA portal to show for it.
FDA to Industry: Review SLP Guides, Gather Data Until MOCRA Portal Launches
October was the deadline but it came and went without a MOCRA portal to show for it. As the industry waits, the FDA advised members to continue collecting data and reviewing guidance documents — including the latest one for Structured Product Labeling.
Nov 3rd, 2023