On 10 March, CFDA unveiled the full context
of the Administrative Measures for Registration of Foods for Special Medical
Purpose. It is specified that FSMP includes those for infant (0-12 months).
Accordingly, this regulation is to be implemented from 1 July.
On 10 March, the China Food and Drug
Administration (CFDA) provided a more detailed version of the Administrative
Measures for Registration of Foods for Special Medical Purpose which it had
earlier issued on 8 December, 2015, with a view to implement from 1 July this
year.
The legislation follows some events last year which pointed to the inadequacy
of the regulatory framework in this area. In August 2015, Jiabili (Hunan) Food
Co., Ltd. - licensed for producing standard infant formula - had its special
infant formula forcibly removed from stores and destroyed.
“In China,
there is only one national standard, the General Rules for Infant Food for
Special Medical Purpose (GB25596-2010), which simply indicates the ratio of
nutrient to be added, but doesn't lay down any detailed rules about examination
and approval of production. So we continued working on the basis of our infant
formula production license,” (awarded on 19 May 2014), a manager from the company
noted, “Previously when the General Administration of Quality Supervision,
Inspection and Quarantine took charge, many dairy companies used the infant
formula production licenses for producing special infant formula. Since the
administration of this subject switched to the CFDA (on 25 December 2013, when
the CFDA published "The infant formula powder production license
examination conditions"), many dairy companies have stopped production as
there are big differences in examination and approval.”
When the revised Law of Food Safety of the People’s Republic of China came into
effect on 1 October, 2015, it required the government to strictly supervise
special foods such as healthcare foods, FSMP (= food for special medical
purpose) and infant foods. From that point, the production and use of FSMP for
infant was specified as different from ordinary food in regulatory terms.
Applicable range for FSMP
The regulation of 10 March first defines the applicable range for FSMP: it is
formula food produced to meet special needs, such as eating limitations,
digestive/adsorption/metabolic disorders and other particular diseases; it
includes formula for infants (0-12 months) and for people above 1 year old.
Special infant formula sold in China include lactose-free and low-lactose
formula, partially and extensively hydrolysed formula, formula for premature
and low birth weight infants and amino acid-based formula for metabolic
disorders.
According to CFDA, manufacturers intending to produce and sell FSMP should:
-
First obtain the relevant business
operation license
-
Complete registration in accordance with
the Administrative Measures for Registration of Foods for Special Medical
Purpose
-
Become licensed for producing FSMP in
accordance with the Administrative Measures for Food Production License
The CFDA is responsible for administration of registration for FSMP via its
affiliated organisations:
-
The Administrative Matters Acceptance and
Report and Complaint Centre, for the acceptance of registration applications
-
The Healthcare Food Examination and
Assessment Centre, for the examination and approval of these applications
-
The Food and Drug Examination and
Inspection Centre, for on-the-spot investigations during the examination of
these applications
-
The provincial food and drug supervision
departments, which should participate in the on-the-spot investigations
New opportunities in specialty infant
formula
For long time, this segment has been dominated by the big 4 multinationals as
such medical-level products present a high barrier to entry due to the related
technological and R&D requirements. However, some domestic infant formula
enterprises have already prepared to register, to seize the new business
opportunities.
On 5 February when Synutra International, Inc. (Synutra) released its Q3 FY2016
(from 1 October to 31 December, 2015) financial figures, the CFO pointed out
that the company’s special formula products will be impacted by the regulation.
However, he claimed: “We are the only producer approved for producing special
infant formula in China. We believe that we are qualified to be the first batch
of enterprises to obtain the production licences in future”.
Currently no enterprises are shown with production licences for producing
special infant formula on the CFDA website, since the regulation has not yet
been issued. In China’s QS website (QS stands for “Qiyeshipin Shengchanxuke” in
pinyin = food production licences for enterprises), only Synutra has a
production license (QS3702 2701 0003) for special lactose-free or low-lactose
infant formula. However, the license expired in June 2014.
Another sign of the changes in this area was the JV announced on 30 October,
2015 between Beingmate Baby & Child Food Co., Ltd. (Beingmate) and Korean
Maeil Dairies Co., Ltd. (Maeil). The JV was set up in early 2016 with
registered capital of USD800,000 (WON1 billion, WON/USD exchange rate @ 0.0008,
sourced on hexun.com), with ownership split 4:6 (= Maeil: Beingmate). It plans
to launch 6 special infant formulas and 8 infant formulas for metabolic
disorder in December this year.
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Tag: infant
formula, dairy